510(k) K851649
K851649 is an FDA 510(k) premarket notification submitted by Photec Diagnostics, Inc. for the device "APO A-I IMMUNOASSAY TEST SET FOR APOLIPOPROTEIN A1". The FDA issued a decision of Substantially Equivalent on June 5, 1985. The device falls under product code DER (Alpha-1-Lipoprotein, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5580. Photec Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 5, 1985
- Date Received
- April 22, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alpha-1-Lipoprotein, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5580
- Review Panel
- IM
- Submission Type