REPRO-MED - THD

FDA Premarket Approval P820034

This medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original pma or panel track supplement and may not represent the most recent labeling.

Pre-market Approval Supplement Details

DeviceREPRO-MED - THD
Generic NameDevice, Testicular Hypothermia
ApplicantREPRO-MED SYSTEMS, INC.
Date Received1982-05-28
Decision Date1984-12-26
Notice Date1985-01-25
PMAP820034
SupplementS
Product CodeLOA 
Docket Number85M-0007
Advisory CommitteeGastroenterology/Urology
Expedited ReviewNo
Combination Product No
Applicant Address REPRO-MED SYSTEMS, INC. 24 Carpenter Rd. chester, NY 10918

Supplemental Filings

Supplement NumberDateSupplement Type
P820034Original Filing
S005 1996-12-12 Normal 180 Day Track
S004 1992-06-08 Normal 180 Day Track
S003 1992-05-14 Normal 180 Day Track
S002 1985-02-04
S001 1985-01-09

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