The following data is part of a premarket notification filed by Tech-co, Inc. with the FDA for Uric Acid.
Device ID | K863924 |
510k Number | K863924 |
Device Name: | URIC ACID |
Classification | Acid, Uric, Uricase (colorimetric) |
Applicant | TECH-CO, INC. 4378 REILLY Troy, MI 48098 |
Contact | Happy Chen |
Correspondent | Happy Chen TECH-CO, INC. 4378 REILLY Troy, MI 48098 |
Product Code | KNK |
CFR Regulation Number | 862.1775 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-08 |
Decision Date | 1986-11-24 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10673486002317 | K863924 | 000 |
10673486002300 | K863924 | 000 |