The following data is part of a premarket notification filed by Pilling Co. with the FDA for Carotid Artery Clamp W/pilling Lmm.
| Device ID | K760646 |
| 510k Number | K760646 |
| Device Name: | CAROTID ARTERY CLAMP W/PILLING LMM |
| Classification | Instruments, Surgical, Cardiovascular |
| Applicant | PILLING CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DWS |
| CFR Regulation Number | 870.4500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-15 |
| Decision Date | 1976-09-21 |