Vital Metrics, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Vital Metrics, Inc.” (first 1982, latest 1988), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 61 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| FFG | Device, Urine Flow Rate Measuring, Non-Electrical, Disposable | 3 | 3 |
| KNX | Collector, Urine, (And Accessories) For Indwelling Catheter | 3 | 3 |
| HBI | Illuminator, Fiberoptic, Surgical Field | 2 | 2 |
Plus 1 more product codes.
Review panels
Most recent Vital Metrics, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K883201 | VITAL-VUE ILLUMINATION, SUCTION & IRRIGATION SYS | HBI | 1988-09-26 | 60 |
| K882956 | VITAL-VUE ILLUMINATION, SUCTION AND IRRIGATION | HBI | 1988-08-03 | 21 |
| K844973 | IRRIGA SUC ILLUM ISIS 710 & 7100 SERIES | — | 1985-03-18 | 84 |
| K843442 | URINARY DRAINAGE CONTAINER 2013 WITH | FFG | 1985-01-03 | 121 |
| K843441 | URINARY DRAINAGE CONTAINER 2012-WITH | FFG | 1985-01-03 | 121 |
| K840917 | URINARY MONITORING SYS 240 | KNX | 1984-05-01 | 61 |
| K834448 | URINARY DRAINAGE CONTAINER | KNX | 1984-02-10 | 56 |
| K832526 | UROTRACK PLUS | KNX | 1983-09-19 | 52 |
| K813641 | VITAL METRICS URINE MONITORING SYSTEM | FFG | 1982-03-01 | 61 |
Recalls
openFDA lists no recalls under a recalling firm named Vital Metrics, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Vital Signs, Inc. (75 510(k)s)
- Vital Images, Inc. (41 510(k)s)
- Vital Diagnostics (Manufacturing) Ptyltd (5 510(k)s)
- Vital Scientific N.V. (5 510(k)s)
- Vital Concepts, Inc. (4 510(k)s)
- Vital Art and Science Incorporated (2 510(k)s)
- Vital Connections, Inc. (2 510(k)s)
- Vital Signs, Inc., A GE Healthcare Company (2 510(k)s)
- Vital 5 (1 510(k)s)
- Vital Access (1 510(k)s)
- Vital Air Oxygen Co. (1 510(k)s)
- Vital Canada, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Vital Metrics, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Vital Metrics, Inc.” (first 1982, latest 1988), across 4 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Vital Metrics, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Vital Metrics, Inc. is 61 days.
Which FDA product codes appear under Vital Metrics, Inc.?
The most frequent FDA product codes under this applicant name are FFG (Device, Urine Flow Rate Measuring, Non-Electrical, Disposable, 3); KNX (Collector, Urine, (And Accessories) For Indwelling Catheter, 3); HBI (Illuminator, Fiberoptic, Surgical Field, 2).
Next steps
- See all 9 Vital Metrics, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FFG, Vital Metrics, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.