510(k) K970314
K970314 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "SYNCHRON LX SYSTEMS APOLIPOPROTEIN (APOA AND APOB) REAGENTS". The FDA issued a decision of Substantially Equivalent on April 21, 1997. The device falls under product code MSJ (Apolipoproteins), a Class I device regulated under 21 CFR 862.1475. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 21, 1997
- Date Received
- January 24, 1997
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Apolipoproteins
- Device Class
- Class I
- Regulation Number
- 862.1475
- Review Panel
- CH
- Submission Type