K882282 is an FDA 510(k) clearance for the SUIT, SURGICAL. This device is classified as a Suit, Surgical (Class I - General Controls, product code FXO).
Submitted by A Plus International, Inc. (La Puente, US). The FDA issued a Cleared decision on June 23, 1988, 23 days after receiving the submission on May 31, 1988.
This device falls under the General Hospital FDA review panel. Regulated under 21 CFR 878.4040.
| 510(k) Number | K882282 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 31, 1988 |
| Decision Date | June 23, 1988 |
| Days to Decision | 23 days |
| Submission Type | Traditional |
| Review Panel | General Hospital (HO) |
| Summary | - |
| Product Code | FXO - Suit, Surgical |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4040 |