The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Uterine Vacum Aspirating Currette.
Device ID | K802360 |
510k Number | K802360 |
Device Name: | UTERINE VACUM ASPIRATING CURRETTE |
Classification | System, Abortion, Vacuum |
Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | HHI |
CFR Regulation Number | 884.5070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1980-09-26 |
Decision Date | 1980-10-31 |