510(k) K862614
K862614 is an FDA 510(k) premarket notification submitted by Gen-Probe, Inc. for the device "RAPID IDENTI. TEST FOR MYCOBACTERIUM TB COMPLEX". The FDA issued a decision of Substantially Equivalent on November 10, 1986. The device falls under product code LQF (Dna-Reagents, Mycobacterium Spp.), a Class I device regulated under 21 CFR 866.3370. Gen-Probe, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 10, 1986
- Date Received
- July 9, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Dna-Reagents, Mycobacterium Spp.
- Device Class
- Class I
- Regulation Number
- 866.3370
- Review Panel
- MI
- Submission Type