510(k) K992430
K992430 is an FDA 510(k) premarket notification submitted by Medical Analysis Systems, Inc. for the device "CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3". The FDA issued a decision of Substantially Equivalent on August 30, 1999. The device falls under product code JJT (Enzyme Controls (Assayed And Unassayed)), a Class I device regulated under 21 CFR 862.1660. Medical Analysis Systems, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 30, 1999
- Date Received
- July 21, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Enzyme Controls (Assayed And Unassayed)
- Device Class
- Class I
- Regulation Number
- 862.1660
- Review Panel
- CH
- Submission Type