Intl. Medical Consultants: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Intl. Medical Consultants” (first 1993, latest 1993), across 1 product code in 1 review panel. Median 510(k) review time under this name: 238 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 |
|---|---|---|---|
| FPA | Set, Administration, Intravascular | 6 | 6 |
Review panels
- General Hospital (6)
Most recent Intl. Medical Consultants 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K931119 | DURHAM; NON CORING WINGED ADMINISTRATION SET | FPA | 1993-11-03 | 244 |
| K930974 | DURHAM; INJECTION SITE EXTENSION SET, LUER LOCK | FPA | 1993-11-03 | 252 |
| K930927 | DURHAM;T ADAPTOR EXTENSIONSET W/INJECTION SITE | FPA | 1993-11-03 | 253 |
| K930926 | DURHAM; Y CHECK SET-LUER LOCK W/INJECTION SITE | FPA | 1993-10-12 | 231 |
| K930751 | DURHAM; EXTENSION TUBE LUER LOCK W/INJECTION SITE | FPA | 1993-09-03 | 203 |
| K930750 | DURHAM; ADM. SET-LUER LOCK W/.22 MICRON FILTER | FPA | 1993-09-03 | 203 |
Recalls
openFDA lists no recalls under a recalling firm named Intl. Medical Consultants.
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.
- Intl. Diagnostic Technology (29 510(k)s)
- Intl. Immunoassay Laboratories, Inc. (27 510(k)s)
- Intl. Medical, Inc. (17 510(k)s)
- Intl. Remote Imaging Systems (14 510(k)s)
- Intl. Medical Devices , Ltd. (12 510(k)s)
- Intl. Playtex, Inc. (10 510(k)s)
- Intl. Business Machines (8 510(k)s)
- Intl. Bioclinical, Inc. (6 510(k)s)
- Intl. Diagnostic, Inc. (6 510(k)s)
- Intl. Medical Equipment Corp. (6 510(k)s)
- Intl. Ophthalmic Industries Corp. (6 510(k)s)
- Intl. Trade Management Co. (6 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Intl. Medical Consultants?
FDA lists 6 510(k) clearances under the applicant name “Intl. Medical Consultants” (first 1993, latest 1993), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Intl. Medical Consultants?
The median time from FDA receipt to decision across 510(k)s cleared under the name Intl. Medical Consultants is 238 days.
Which FDA product codes appear under Intl. Medical Consultants?
The most frequent FDA product codes under this applicant name are FPA (Set, Administration, Intravascular, 6).
Next steps
- See all 6 Intl. Medical Consultants clearances with predicates and recalls
- Run predicate analysis for product code FPA, Intl. Medical Consultants'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.