510(k) K890089

RAPID DIAG. SYSTEM FOR MYCOBACTERIUM GORDONAE by Gen-Probe, Inc. — Product Code LQF

K890089 is an FDA 510(k) premarket notification submitted by Gen-Probe, Inc. for the device "RAPID DIAG. SYSTEM FOR MYCOBACTERIUM GORDONAE". The FDA issued a decision of Substantially Equivalent on March 13, 1989. 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
March 13, 1989
Date Received
January 10, 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