The following data is part of a premarket notification filed by Data Medical Associates, Inc. with the FDA for Uric Acid Procedure.
| Device ID | K861660 |
| 510k Number | K861660 |
| Device Name: | URIC ACID PROCEDURE |
| Classification | Acid, Uric, Uricase (colorimetric) |
| Applicant | DATA MEDICAL ASSOCIATES, INC. 845 AVENUE G EAST Arlington, TX 76011 |
| Contact | Jerry A Graham |
| Correspondent | Jerry A Graham DATA MEDICAL ASSOCIATES, INC. 845 AVENUE G EAST Arlington, TX 76011 |
| Product Code | KNK |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-04-30 |
| Decision Date | 1986-06-13 |