510(k) K020282
K020282 is an FDA 510(k) premarket notification submitted by Jas Diagnostics, Inc. for the device "JAS AMYLASE LIQUID REAGENT". The FDA issued a decision of Substantially Equivalent on February 28, 2002. The device falls under product code JFJ (Catalytic Methods, Amylase), a Class II device regulated under 21 CFR 862.1070. Jas Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 28, 2002
- Date Received
- January 28, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catalytic Methods, Amylase
- Device Class
- Class II
- Regulation Number
- 862.1070
- Review Panel
- CH
- Submission Type