510(k) K862614

RAPID IDENTI. TEST FOR MYCOBACTERIUM TB COMPLEX by Gen-Probe, Inc. — Product Code LQF

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