Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Apothecary Products, Inc. · Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
141 daysmedian FDA review time
149 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K140409 | FLENTS PLASTIC EYE WASH CUP | Apothecary Products, Inc. | 2014-07-09 | 141 | 0 |
| K111856 | SOFT GRIP CONTACT LENS CASE, DELUXE CONTACT LENS CASE, ECONO | Apothecary Products, Inc. | 2011-07-14 | 15 | 0 |
| K041766 | EZY-TRAVEL WRISTBAND | Apothecary Products, Inc. | 2004-11-26 | 149 | 0 |
| K020296 | ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057 | Apothecary Products, Inc. | 2002-06-25 | 148 | 0 |
| K892242 | PATIENT EXAMINATION GLOVES (LATEX) | Apothecary Products, Inc. | 1989-05-12 | 37 | 0 |
| K833311 | NITROGLYCERINE CONTAINER | Apothecary Products, Inc. | 1984-02-04 | 131 | 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