FDA 510(k) Application Details - K962217

Device Classification Name	Dna Probe, Nucleic Acid Amplification, Chlamydia   More FDA Info for this Device
510(K) Number	K962217
Device Name	Dna Probe, Nucleic Acid Amplification, Chlamydia
Applicant	GEN-PROBE, INC. 9880 CAMPUS POINT DR. SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	GERALD H SCHELL Other 510(k) Applications for this Contact
Regulation Number	866.3120   More FDA Info for this Regulation Number
Classification Product Code	MKZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/10/1996
Decision Date	11/27/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	MI - Microbiology
Review Advisory Committee	MI - Microbiology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review