510(k) K831377
K831377 is an FDA 510(k) premarket notification submitted by American Diagnostic Corp. for the device "IGE RADIOIMMUNOASSAY KIT". The FDA issued a decision of Substantially Equivalent on June 2, 1983. The device falls under product code DGC (Ige, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. American Diagnostic Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 1983
- Date Received
- April 27, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ige, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- IM
- Submission Type