Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medical Marketing Group — Predicate Candidate Screening
11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
35 daysmedian FDA review time
91 days90th percentile
11clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K910022 | MMG/O'NEIL URINARY CATHETERIZATION SYSTEM KIT | Medical Marketing Group | 1991-04-02 | 89 | 0 |
| K884819 | O'NEIL URINARY CATHETER INTRODUCER | Medical Marketing Group | 1989-02-17 | 92 | 0 |
| K874682 | MMG CATHETER PLUG W/DRAINAGE TUBE COVER | Medical Marketing Group | 1988-01-27 | 75 | 0 |
| K871999 | MMG URO-SELF CATHETER | Medical Marketing Group | 1987-08-25 | 91 | 0 |
| K863912 | THE MMG 5 IN 1 CONNECTOR | Medical Marketing Group | 1986-10-27 | 19 | 0 |
| K840838 | MMG CONNECTIVE TUBING | Medical Marketing Group | 1984-03-30 | 35 | 0 |
| K821168 | DISPOSABLE URINARY LEGBAG W/STRAP | Medical Marketing Group | 1982-05-24 | 27 | 0 |
| K811469 | MMG URINARY DRAINAGE TUBING | Medical Marketing Group | 1981-06-12 | 17 | 0 |
| K800694 | MMG DISPOSABLE URINARY LEG BAG | Medical Marketing Group | 1980-05-30 | 64 | 0 |
| K791847 | ASPRI-LUKE | Medical Marketing Group | 1979-10-02 | 13 | 0 |
| K790279 | CATHETER, MMG LATEX EXTERNAL | Medical Marketing Group | 1979-03-06 | 21 | 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