Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Moss Medical Products — Predicate Candidate Screening
8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
175 daysmedian FDA review time
459 days90th percentile
8clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K051206 | Y2K2 ENTERNAL TUBE FLUID FILTER | Moss Medical Products | 2005-11-02 | 175 | 0 |
| K030413 | Y2K2 ENTERNAL FEEDING MANAGER | Moss Medical Products | 2004-05-11 | 459 | 0 |
| K031492 | MOSSMED DUAL INTERMITTENT ASPIRATOR | Moss Medical Products | 2004-02-05 | 269 | 0 |
| K913701 | MOSS - ANCHOR SET | Moss Medical Products | 1992-02-14 | 179 | 0 |
| K910910 | MOSS- ANCHOR SET | Moss Medical Products | 1991-06-24 | 111 | 0 |
| K910912 | MOSS NASAL TUBE MARK IV | Moss Medical Products | 1991-05-28 | 84 | 0 |
| K910911 | MOSS P.E.G. TRAY | Moss Medical Products | 1991-05-03 | 59 | 0 |
| K910913 | MOSS GASTROSTOMY TUBE | Moss Medical Products | 1991-04-19 | 45 | 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