Daily Medical Products, Inc.: FDA filings under this applicant name
FDA lists 8 510(k) clearances under the applicant name “Daily Medical Products, Inc.” (first 1990, latest 1992), across 3 product codes in 2 review panels. Median 510(k) review time under this name: 54 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 |
|---|---|---|---|
| DWC | Controller, Temperature, Cardiopulmonary Bypass | 5 | 5 |
| FLL | Continuous Measurement Thermometer | 2 | 2 |
| DTR | Heat-Exchanger, Cardiopulmonary Bypass | 1 | 1 |
Review panels
- Cardiovascular (6)
- General Hospital (2)
Most recent Daily Medical Products, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K914005 | FIBEROPTIC TYMPANIC THERMOMETER, MODEL 6000 | FLL | 1992-07-30 | 328 |
| K905652 | MYOCARDIAL TEMPERATURE MONITORING PROBES, CJ-1000 | FLL | 1991-02-14 | 58 |
| K905568 | TOPICAL COOLING PAD, MODEL 7000 | DTR | 1991-01-23 | 42 |
| K896975 | CARDIAC COOLING JACKET, 30% REDUCED, MODEL CJ-220 | DWC | 1990-02-05 | 54 |
| K896974 | CARDIAC COOLING JACKET, 8 CM, MODEL CJ-120 | DWC | 1990-02-05 | 54 |
| K896973 | CARDIAC COOLING JACKET, 30% ENLARGED, MODEL CJ-320 | DWC | 1990-02-05 | 54 |
| K896972 | CARDIAC COOLING JACKET, 12 CM, MODEL CJ-520 | DWC | 1990-02-05 | 54 |
| K896971 | CARDIAC COOLING JACKET, 8 CM, MODEL CJ-420 | DWC | 1990-02-05 | 54 |
Recalls
openFDA lists no recalls under a recalling firm named Daily Medical Products, 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.
- Daily Medical, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Daily Medical Products, Inc.?
FDA lists 8 510(k) clearances under the applicant name “Daily Medical Products, Inc.” (first 1990, latest 1992), across 3 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 Daily Medical Products, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Daily Medical Products, Inc. is 54 days.
Which FDA product codes appear under Daily Medical Products, Inc.?
The most frequent FDA product codes under this applicant name are DWC (Controller, Temperature, Cardiopulmonary Bypass, 5); FLL (Continuous Measurement Thermometer, 2); DTR (Heat-Exchanger, Cardiopulmonary Bypass, 1).
Next steps
- See all 8 Daily Medical Products, Inc. clearances with predicates and recalls
- Run predicate analysis for product code DWC, Daily Medical Products, 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.