K760453 is an FDA 510(k) clearance for the REGULATOR, PRESSURE, CUFF. This device is classified as a Tube Tracheostomy And Tube Cuff (Class II - Special Controls, product code JOH).
Submitted by Boehringer Laboratories (Mchenry, US). The FDA issued a Cleared decision on September 13, 1976, 28 days after receiving the submission on August 16, 1976.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5800.
| 510(k) Number | K760453 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 16, 1976 |
| Decision Date | September 13, 1976 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | JOH — Tube Tracheostomy And Tube Cuff |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5800 |