Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Clinical Convenience Products, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
28 daysmedian FDA review time
340 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K934759 | CULTURIA MACCONKEY-MUG | Clinical Convenience Products, Inc. | 1994-09-09 | 340 | 0 |
| K870502 | CULTURIA MACCONKEY-MUG/MODIFIED TSA SYSTEMS | Clinical Convenience Products, Inc. | 1987-02-26 | 22 | 0 |
| K864764 | CULTURIA MACCONKEY-MUG/CLED SYSTEMS | Clinical Convenience Products, Inc. | 1986-12-29 | 24 | 0 |
| K800215 | CULTURIA MACCONKEY/CLED #DM87 | Clinical Convenience Products, Inc. | 1980-02-13 | 9 | 0 |
| K792579 | CULTURIA MACCONKEY/COLUMBIA CNA | Clinical Convenience Products, Inc. | 1980-01-11 | 28 | 0 |
| K792284 | CULTURIA EMB/COLUMBIA CNA W/5% SHEEP | Clinical Convenience Products, Inc. | 1979-12-19 | 36 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda