The following data is part of a premarket notification filed by American Endoscopy, Inc. with the FDA for E.r.c.p. Cannulas.
| Device ID | K820431 |
| 510k Number | K820431 |
| Device Name: | E.R.C.P. CANNULAS |
| Classification | Endoscopic Retrograde Cholangiopancreatography (ercp) Cannula |
| Applicant | AMERICAN ENDOSCOPY, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ODD |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-02-17 |
| Decision Date | 1982-04-09 |