510(k) K943194
K943194 is an FDA 510(k) premarket notification submitted by Diagnostic Products Corp. for the device "IMMULITE(R) ALLERGY FOOD PANEL FP5E". The FDA issued a decision of Substantially Equivalent on February 23, 1995. The device falls under product code DGO (Ige, Peroxidase, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Diagnostic Products Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 23, 1995
- Date Received
- July 5, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ige, Peroxidase, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- PA
- Submission Type