510(k) K994140
K994140 is an FDA 510(k) premarket notification submitted by Nichols Institute Diagnostics for the device "NICHOLS CHEMILUMINESCENCE THYROGLOBULIN, MODEL 60-4240". The FDA issued a decision of Substantially Equivalent on May 9, 2000. The device falls under product code MSW (System, Test, Thyroglobulin), a Class II device regulated under 21 CFR 866.6010. Nichols Institute Diagnostics has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 2000
- Date Received
- December 8, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, Thyroglobulin
- Device Class
- Class II
- Regulation Number
- 866.6010
- Review Panel
- IM
- Submission Type