K853965 is an FDA 510(k) clearance for the NEOGUARD CHEST PERCUSSOR. This device is classified as a Percussor, Powered-electric (Class II - Special Controls, product code BYI).
Submitted by Cas Medical Systems, Inc. (Branford, US). The FDA issued a Cleared decision on December 3, 1985, 68 days after receiving the submission on September 26, 1985.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5665.
| 510(k) Number | K853965 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 26, 1985 |
| Decision Date | December 03, 1985 |
| Days to Decision | 68 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | - |
| Product Code | BYI - Percussor, Powered-electric |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5665 |