The following data is part of a premarket notification filed by Cooper Medical Devices Corp. with the FDA for Vabra Aspirator.
| Device ID | K800833 |
| 510k Number | K800833 |
| Device Name: | VABRA ASPIRATOR |
| Classification | System, Abortion, Vacuum |
| Applicant | COOPER MEDICAL DEVICES 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 | 1980-04-14 |
| Decision Date | 1980-05-14 |