510(k) K963680
K963680 is an FDA 510(k) premarket notification submitted by Texas Immunology, Inc. for the device "TARGET MYOGLOBIN TEST". The FDA issued a decision of Substantially Equivalent on February 6, 1997. The device falls under product code DDR (Myoglobin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5680. Texas Immunology, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 6, 1997
- Date Received
- September 16, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Myoglobin, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5680
- Review Panel
- IM
- Submission Type