The following data is part of a premarket notification filed by Brimfield Scientific Instruments with the FDA for Brimfield Cannulated Magnetic Retriever.
| Device ID | K843135 |
| 510k Number | K843135 |
| Device Name: | BRIMFIELD CANNULATED MAGNETIC RETRIEVER |
| Classification | Endoscopic Magnetic Retriever |
| Applicant | BRIMFIELD SCIENTIFIC INSTRUMENTS 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FCC |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-08-09 |
| Decision Date | 1984-09-26 |