The following data is part of a premarket notification filed by Safetex Corp. with the FDA for Saxon Ribbed Condoms.
Device ID | K902509 |
510k Number | K902509 |
Device Name: | SAXON RIBBED CONDOMS |
Classification | Condom |
Applicant | SAFETEX CORP. 16101 CONTINENTAL BLVD. Colonial Heights, VA 23834 |
Contact | Ronald L Davis |
Correspondent | Ronald L Davis SAFETEX CORP. 16101 CONTINENTAL BLVD. Colonial Heights, VA 23834 |
Product Code | HIS |
CFR Regulation Number | 884.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-05 |
Decision Date | 1990-07-24 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10302340096581 | K902509 | 000 |
00023400824403 | K902509 | 000 |