Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Medical Measurements, Inc. · Predicate Candidate Screening
8 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
30 daysmedian FDA review time
147 days90th percentile
8clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K921062 | GAELTEC MPR SERIES | Medical Measurements, Inc. | 1992-07-30 | 147 | 0 |
| K902097 | MODEL TR RECTAL SUCTION BIOPSY TUBE | Medical Measurements, Inc. | 1990-07-27 | 80 | 0 |
| K863479 | MODIFIED ICT/B INTRACRANIAL PRESS. TRANS. EPIDURAL | Medical Measurements, Inc. | 1986-10-14 | 35 | 0 |
| K801757 | MMI/GAELTEC CATHETER TIP PRESS. TRANSDU | Medical Measurements, Inc. | 1980-08-27 | 30 | 0 |
| K801756 | MMI/GAELTEC CATHETER TIP TRANSDUC | Medical Measurements, Inc. | 1980-08-20 | 23 | 0 |
| K801880 | MMI/GAELTEC SERIES 8T DIFF. PRESS. TRANS | Medical Measurements, Inc. | 1980-08-14 | 7 | 0 |
| K801758 | MMI/GAELTEC CATHETER INTRAUTERINE | Medical Measurements, Inc. | 1980-08-14 | 17 | 0 |
| K801755 | MMI/GAELTEC CATHETER TIP PRESSURE | Medical Measurements, Inc. | 1980-08-13 | 16 | 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