510(k) K897077

ACCUPROBE MYCOBACTERIUM INTRACELLULARE CULTURE by Gen-Probe, Inc. — Product Code LQF

K897077 is an FDA 510(k) premarket notification submitted by Gen-Probe, Inc. for the device "ACCUPROBE MYCOBACTERIUM INTRACELLULARE CULTURE". The FDA issued a decision of Substantially Equivalent on August 23, 1990. 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
August 23, 1990
Date Received
December 22, 1989
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