The following data is part of a premarket notification filed by Conphar, Inc. with the FDA for Conphar Percussion Hammer(taylor).
| Device ID | K803148 |
| 510k Number | K803148 |
| Device Name: | CONPHAR PERCUSSION HAMMER(TAYLOR) |
| Classification | Percussor |
| Applicant | CONPHAR, INC. 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 | 1980-12-12 |
| Decision Date | 1981-01-08 |