The following data is part of a premarket notification filed by Williams Specialty Products, Inc. with the FDA for Cannula, Suction Uterine.
| Device ID | K900641 |
| 510k Number | K900641 |
| Device Name: | CANNULA, SUCTION UTERINE |
| Classification | System, Abortion, Vacuum |
| Applicant | WILLIAMS SPECIALTY PRODUCTS, INC. 3700 WESTFALL DR. Encino, CA 91436 |
| Contact | Williams, Md |
| Correspondent | Williams, Md WILLIAMS SPECIALTY PRODUCTS, INC. 3700 WESTFALL DR. Encino, CA 91436 |
| Product Code | HHI |
| CFR Regulation Number | 884.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-02-09 |
| Decision Date | 1990-03-30 |