K852102 is an FDA 510(k) clearance for the COLLIN BODY PLETHYSMOGRAPH PLUS SYSTEM. This device is classified as a Plethysmograph, Pressure (Class II - Special Controls, product code CCM).
Submitted by Warren E. Collins, Inc. (Braintree, US). The FDA issued a Cleared decision on July 31, 1985, 77 days after receiving the submission on May 15, 1985.
This device falls under the Anesthesiology FDA review panel. Regulated under 21 CFR 868.1750.
| 510(k) Number | K852102 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 15, 1985 |
| Decision Date | July 31, 1985 |
| Days to Decision | 77 days |
| Submission Type | Traditional |
| Review Panel | Anesthesiology (AN) |
| Summary | — |
| Product Code | CCM — Plethysmograph, Pressure |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 868.1750 |