510(k) K895648
K895648 is an FDA 510(k) premarket notification submitted by Ventrex Laboratories, Inc. for the device "COATED TUBE HIGH SENSITIVITY TSH 100 UIU/ML STAN.". The FDA issued a decision of Substantially Equivalent on January 18, 1990. The device falls under product code JIT (Calibrator, Secondary), a Class II device regulated under 21 CFR 862.1150. Ventrex Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 18, 1990
- Date Received
- September 20, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calibrator, Secondary
- Device Class
- Class II
- Regulation Number
- 862.1150
- Review Panel
- CH
- Submission Type