The following data is part of a premarket notification filed by Cosmedtech, Inc. with the FDA for Cannula And General Purpose Aspirator.
| Device ID | K873552 |
| 510k Number | K873552 |
| Device Name: | CANNULA AND GENERAL PURPOSE ASPIRATOR |
| Classification | System, Abortion, Vacuum |
| Applicant | COSMEDTECH, INC. 25625 MINOA DR. Mission Viejo, CA 92691 |
| Contact | John M Nordlund |
| Correspondent | John M Nordlund COSMEDTECH, INC. 25625 MINOA DR. Mission Viejo, CA 92691 |
| Product Code | HHI |
| CFR Regulation Number | 884.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-08-10 |
| Decision Date | 1987-11-25 |