510(k) K812453
K812453 is an FDA 510(k) premarket notification submitted by Scripps-Miles, Inc. for the device "SCRIPPSYSTEM IMMUNOGLOBIN RID KIT". The FDA issued a decision of Substantially Equivalent on September 23, 1981. The device falls under product code DEW (Igg, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5510. Scripps-Miles, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 23, 1981
- Date Received
- August 28, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Igg, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- IM
- Submission Type