The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Curette, Uterine, Vacuum Aspirating.
| Device ID | K770674 |
| 510k Number | K770674 |
| Device Name: | CURETTE, UTERINE, VACUUM ASPIRATING |
| Classification | Curette, Suction, Endometrial (and Accessories) |
| Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | HHK |
| CFR Regulation Number | 884.1175 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-04-11 |
| Decision Date | 1977-04-26 |