The following data is part of a premarket notification filed by A.p. Total Care, Inc. with the FDA for Uric Acid, Model Ua112-01.
Device ID | K991247 |
510k Number | K991247 |
Device Name: | URIC ACID, MODEL UA112-01 |
Classification | Acid, Uric, Uricase (colorimetric) |
Applicant | A.P. TOTAL CARE, INC. 70 HAWLEY AVE, PO BOX 6216 Bridgeport, CT |
Contact | Luis P Leon |
Correspondent | Luis P Leon A.P. TOTAL CARE, INC. 70 HAWLEY AVE, PO BOX 6216 Bridgeport, CT |
Product Code | KNK |
CFR Regulation Number | 862.1775 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-04-12 |
Decision Date | 1999-05-25 |