The following data is part of a premarket notification filed by Northgate Technologies, Inc. with the FDA for Aspiration/injection Needle.
| Device ID | K913992 |
| 510k Number | K913992 |
| Device Name: | ASPIRATION/INJECTION NEEDLE |
| Classification | Needle, Aspiration And Injection, Disposable |
| Applicant | NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights, IL 60004 |
| Contact | Peter A Manzie |
| Correspondent | Peter A Manzie NORTHGATE TECHNOLOGIES, INC. 3930 VENTURA DR. Arlington Heights, IL 60004 |
| Product Code | GAA |
| CFR Regulation Number | 878.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-05 |
| Decision Date | 1991-10-30 |