K023704 is an FDA 510(k) clearance for the KSEA SCB ACC CONTROL. This device is classified as a Light, Surgical, Accessories (Class II - Special Controls, product code FTA).
Submitted by KARL STORZ Endoscopy-America, Inc. (Culver City, US). The FDA issued a Cleared decision on January 30, 2003, 87 days after receiving the submission on November 4, 2002.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4580.
| 510(k) Number | K023704 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 04, 2002 |
| Decision Date | January 30, 2003 |
| Days to Decision | 87 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | FTA — Light, Surgical, Accessories |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4580 |