K973621 is an FDA 510(k) clearance for the PRE-VIEW CHOLANGIOGRAPHY CLAMP, a Catheter, Cholangiography (Class I — General Controls, product code GBZ), submitted by Nashville Surgical Instruments (Springfield, US). The FDA issued a Cleared decision on December 17, 1997, 85 days after receiving the submission on September 23, 1997. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K973621 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 23, 1997 |
| Decision Date | December 17, 1997 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GBZ — Catheter, Cholangiography |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 878.4200 |