510(k) K965100
K965100 is an FDA 510(k) premarket notification submitted by Crestat Diagnostics, Inc. for the device "N-ASSAY TIA ALPHA-1-ANTITRYPSIN TEST KIT". The FDA issued a decision of Substantially Equivalent on July 14, 1997. The device falls under product code DEM (Alpha-1-Antitrypsin, Antigen, Antiserum, Control), a Class II device regulated under 21 CFR 866.5130. Crestat Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 14, 1997
- Date Received
- December 20, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Alpha-1-Antitrypsin, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5130
- Review Panel
- IM
- Submission Type