K781908 is an FDA 510(k) clearance for the BREATHING CIRCUIT PRODUCTS, ANESTHESIA. This device is classified as a Circuit, Breathing (w Connector, Adaptor, Y Piece) (Class I - General Controls, product code CAI).
Submitted by Hospitak, Inc. (Walker, US). The FDA issued a Cleared decision on November 27, 1978, 13 days after receiving the submission on November 14, 1978.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5240.
| 510(k) Number | K781908 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 14, 1978 |
| Decision Date | November 27, 1978 |
| Days to Decision | 13 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CAI — Circuit, Breathing (w Connector, Adaptor, Y Piece) |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 868.5240 |