PMA P890064S002

Device
VIRATYPE HUMAN PAPILLOMAVIRUS DNA TYPING KIT
Applicant
Qiagen Gaithersburg, Inc.
PMA number
P890064
Supplement
S002
Product code
MAQ
Decision date
1994-05-19
Classification
Kit, Dna Detection, Human Papillomavirus
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS

Current openFDA PMA Record#

Device
VIRATYPE HUMAN PAPILLOMAVIRUS DNA TYPING KIT
Applicant
Qiagen Gaithersburg, Inc.
PMA number
P890064
Supplement
S002
Product code
MAQ
Generic name
KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
Decision date
1994-05-19
Decision code
APPR
Date received
1992-12-09
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material