K060657 is an FDA 510(k) clearance for the ISLEEP BY BREAS, MODELS ISLEEP 10, ISLEEP 20.. This device is classified as a Ventilator, Non-continuous (respirator) (Class II - Special Controls, product code BZD).
Submitted by Breas Medical AB (Molnlycke, SE). The FDA issued a Cleared decision on August 18, 2006, 158 days after receiving the submission on March 13, 2006.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.5905.
| 510(k) Number | K060657 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 13, 2006 |
| Decision Date | August 18, 2006 |
| Days to Decision | 158 days |
| Submission Type | Special |
| Review Panel | Anesthesiology (AN) |
| Summary | Summary PDF |
| Product Code | BZD — Ventilator, Non-continuous (respirator) |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.5905 |