The following data is part of a premarket notification filed by Catachem, Inc. with the FDA for Uric Acid For Manual/automated Applications.
| Device ID | K895821 |
| 510k Number | K895821 |
| Device Name: | URIC ACID FOR MANUAL/AUTOMATED APPLICATIONS |
| Classification | Acid, Uric, Uricase (colorimetric) |
| Applicant | CATACHEM, INC. 6 NORTH PEARL ST. Port Chester, NY 10573 |
| Contact | Luis P Leon |
| Correspondent | Luis P Leon CATACHEM, INC. 6 NORTH PEARL ST. Port Chester, NY 10573 |
| Product Code | KNK |
| CFR Regulation Number | 862.1775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-09-29 |
| Decision Date | 1989-12-05 |