510(k) K900449
K900449 is an FDA 510(k) premarket notification submitted by Pharmacia, Inc. for the device "PHARMACIA B2 MICRO EIA". The FDA issued a decision of Substantially Equivalent on February 5, 1990. The device falls under product code JZG (System, Test, Beta-2-Microglobulin Immunological), a Class II device regulated under 21 CFR 866.5630. Pharmacia, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 5, 1990
- Date Received
- January 30, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, Beta-2-Microglobulin Immunological
- Device Class
- Class II
- Regulation Number
- 866.5630
- Review Panel
- IM
- Submission Type