Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Camino Neurocare, 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) |
|---|---|---|---|---|---|
| K982702 | VENTRIX SUBDURAL TUNNELING PRESSURE MONITORING KIT MODEL NL9 | Camino Neurocare, Inc. | 1998-09-10 | 38 | 0 |
| K981846 | PARENCHYMAL BOLT PRESSURE MONITORING KIT | Camino Neurocare, Inc. | 1998-08-18 | 84 | 0 |
| K962928 | COMBINED INTRACRANIAL PRESSURE-TEMPERATURE SENSING SYSTEM (I | Camino Neurocare, Inc. | 1996-12-20 | 144 | 2 |
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