510(k) K990073
K990073 is an FDA 510(k) premarket notification submitted by Kmi Diagnostics, Inc. for the device "CALCITONIN". The FDA issued a decision of Substantially Equivalent on May 11, 1999. The device falls under product code JKR (Radioimmunoassay, Calcitonin), a Class II device regulated under 21 CFR 862.1140. Kmi Diagnostics, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 11, 1999
- Date Received
- January 11, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Radioimmunoassay, Calcitonin
- Device Class
- Class II
- Regulation Number
- 862.1140
- Review Panel
- CH
- Submission Type