K913000 is an FDA 510(k) clearance for the HEART NEBULIZER POLE CLAMP. This device is classified as a Nebulizer (direct Patient Interface) (Class II - Special Controls, product code CAF).
Submitted by B&B Medical Technologies, Inc. (Orangevale, US). The FDA issued a Cleared decision on August 2, 1991, 25 days after receiving the submission on July 8, 1991.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5630.
| 510(k) Number | K913000 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 08, 1991 |
| Decision Date | August 02, 1991 |
| Days to Decision | 25 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | Statement |
| Product Code | CAF — Nebulizer (direct Patient Interface) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5630 |