510(k) K921435

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

K921435 is an FDA 510(k) premarket notification submitted by Gen-Probe, Inc. for the device "ACCUPROBE MYCOBACTERIUM AVIUM COMPLEX CULTURE". The FDA issued a decision of Substantially Equivalent on July 23, 1992. 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 23, 1992
Date Received
March 25, 1992
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