510(k) K871795

RAPID DIAGNOSTIC SYSTEM FOR MYCOBACTERIUM TUBER. by Gen-Probe, Inc. — Product Code LQF

K871795 is an FDA 510(k) premarket notification submitted by Gen-Probe, Inc. for the device "RAPID DIAGNOSTIC SYSTEM FOR MYCOBACTERIUM TUBER.". The FDA issued a decision of Substantially Equivalent on July 30, 1987. 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
July 30, 1987
Date Received
May 7, 1987
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