The following data is part of a premarket notification filed by Rms Div. with the FDA for Dw234 #29.
| Device ID | K941625 |
| 510k Number | K941625 |
| Device Name: | DW234 #29 |
| Classification | Alloy, Other Noble Metal |
| Applicant | RMS DIV. 175 PINEVIEW DR. Amherst, NY 14228 |
| Contact | Lloyd V Ziemendorf |
| Correspondent | Lloyd V Ziemendorf RMS DIV. 175 PINEVIEW DR. Amherst, NY 14228 |
| Product Code | EJS |
| CFR Regulation Number | 872.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-04-04 |
| Decision Date | 1994-06-22 |