The following data is part of a premarket notification filed by Amdia Medical Products with the FDA for Bucks Neurological Hammer.
| Device ID | K791336 |
| 510k Number | K791336 |
| Device Name: | BUCKS NEUROLOGICAL HAMMER |
| Classification | Percussor |
| Applicant | AMDIA MEDICAL PRODUCTS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GWZ |
| CFR Regulation Number | 882.1700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-07-20 |
| Decision Date | 1979-08-03 |