510(k) K896867
K896867 is an FDA 510(k) premarket notification submitted by In Vitro Diagnostics, Inc. for the device "THYROID STIMULATING HORMONE-EIA-XT". The FDA issued a decision of Substantially Equivalent on February 23, 1990. The device falls under product code JLW (Radioimmunoassay, Thyroid-Stimulating Hormone), a Class II device regulated under 21 CFR 862.1690. In Vitro Diagnostics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 23, 1990
- Date Received
- December 6, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Thyroid-Stimulating Hormone
- Device Class
- Class II
- Regulation Number
- 862.1690
- Review Panel
- CH
- Submission Type