SAXON RIBBED CONDOMS

Condom

SAFETEX CORP.

The following data is part of a premarket notification filed by Safetex Corp. with the FDA for Saxon Ribbed Condoms.

Pre-market Notification Details

Device IDK902509
510k NumberK902509
Device Name:SAXON RIBBED CONDOMS
ClassificationCondom
Applicant SAFETEX CORP. 16101 CONTINENTAL BLVD. Colonial Heights,  VA  23834
ContactRonald L Davis
CorrespondentRonald L Davis
SAFETEX CORP. 16101 CONTINENTAL BLVD. Colonial Heights,  VA  23834
Product CodeHIS  
CFR Regulation Number884.5300 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1990-06-05
Decision Date1990-07-24

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10302340096581 K902509 000
00023400824403 K902509 000

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