510(k) K933078
K933078 is an FDA 510(k) premarket notification submitted by Beckman Instruments, Inc. for the device "BECKMAN ALPHA-1-MICROGLOBULIN (A1M) REAGENT". The FDA issued a decision of Substantially Equivalent on January 11, 1994. The device falls under product code MGA (Alpha-1 Microglobulin, Antigen, Antiserum, Control), a Class I device regulated under 21 CFR 866.5400. Beckman Instruments, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 11, 1994
- Date Received
- June 23, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alpha-1 Microglobulin, Antigen, Antiserum, Control
- Device Class
- Class I
- Regulation Number
- 866.5400
- Review Panel
- IM
- Submission Type