510(k) K020454
K020454 is an FDA 510(k) premarket notification submitted by Jas Diagnostics, Inc. for the device "CHEMISTRY CALIBRATOR". The FDA issued a decision of Substantially Equivalent on April 8, 2002. The device falls under product code JIT (Calibrator, Secondary), a Class II device regulated under 21 CFR 862.1150. Jas Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 8, 2002
- Date Received
- February 11, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calibrator, Secondary
- Device Class
- Class II
- Regulation Number
- 862.1150
- Review Panel
- CH
- Submission Type