The following data is part of a premarket notification filed by Squibb & Sons, Inc. with the FDA for Angiotensin I Immutope Kit.
| Device ID | K761267 |
| 510k Number | K761267 |
| Device Name: | ANGIOTENSIN I IMMUTOPE KIT |
| Classification | Radioimmunoassay, Angiotensin I And Renin |
| Applicant | SQUIBB & SONS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | CIB |
| CFR Regulation Number | 862.1085 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-12-16 |
| Decision Date | 1976-12-30 |