Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Chestnut Medical Technologies, Inc. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K093977 | ALLIGATOR-HD RETRIEVAL DEVICE (ARD-HD), MODEL FA-88840-XX | Chestnut Medical Technologies, Inc. | 2010-04-22 | 119 | 0 |
| K091559 | MARKSMANN CATHETER | Chestnut Medical Technologies, Inc. | 2009-09-18 | 113 | 0 |
| K043580 | ALLIGATOR RETRIEVAL DEVICE (ARD) | Chestnut Medical Technologies, Inc. | 2005-03-24 | 86 | 1 |
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