Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Intl. Medical Marketing, Inc. · Predicate Candidate Screening
5 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
89 daysmedian FDA review time
165 days90th percentile
5clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K897181 | L.T.C. PERCUTANEOUS ENDOSCOPIC GASTROSTOMY TUBE | Intl. Medical Marketing, Inc. | 1990-03-27 | 89 | 0 |
| K895824 | L.T.C. ENTERAL BAG ADMINISTRATION SET W/PUMP SET | Intl. Medical Marketing, Inc. | 1990-03-13 | 165 | 0 |
| K896621 | L.T.C. REPLACEMENT GASTROSTOMY TUBE | Intl. Medical Marketing, Inc. | 1990-03-13 | 112 | 0 |
| K895616 | L.T.C. FEEDING TUBE | Intl. Medical Marketing, Inc. | 1989-10-24 | 35 | 0 |
| K895957 | L.T.C. 1000 URINARY DRAINAGE BAG | Intl. Medical Marketing, Inc. | 1989-10-24 | 13 | 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