K944790 is an FDA 510(k) clearance for the FLEXIBLE LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER. This device is classified as a Catheter, Cholangiography (Class I - General Controls, product code GBZ).
Submitted by Applied Medical Resources (Launa Hills, US). The FDA issued a Cleared decision on November 29, 1994, 62 days after receiving the submission on September 28, 1994.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4200.
| 510(k) Number | K944790 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 28, 1994 |
| Decision Date | November 29, 1994 |
| Days to Decision | 62 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 |