510(k) K883726
K883726 is an FDA 510(k) premarket notification submitted by Immuchem Corp. for the device "THYROID STIMULATING HORMONE (HTSH) IRMA NEONATAL". The FDA issued a decision of Substantially Equivalent on December 15, 1988. The device falls under product code JLW (Radioimmunoassay, Thyroid-Stimulating Hormone), a Class II device regulated under 21 CFR 862.1690. Immuchem Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 15, 1988
- Date Received
- August 31, 1988
- 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