Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
General Meditech, Inc. · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K092970 | GENERAL PATIENT MONITORS, MODELS: G3C/ G3D/ G3F/ G3G/ G3H | General Meditech, Inc. | 2010-02-02 | 130 | 0 |
| K082789 | G1B PULSE OXIMETER | General Meditech, Inc. | 2009-01-07 | 106 | 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