510(k) K012038
K012038 is an FDA 510(k) premarket notification submitted by Jas Diagnostics, Inc. for the device "JAS URIC ACID LIQUID REAGENT". The FDA issued a decision of Substantially Equivalent on August 21, 2001. The device falls under product code KNK (Acid, Uric, Uricase (Colorimetric)), a Class I device regulated under 21 CFR 862.1775. Jas Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 21, 2001
- Date Received
- June 29, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Acid, Uric, Uricase (Colorimetric)
- Device Class
- Class I
- Regulation Number
- 862.1775
- Review Panel
- CH
- Submission Type