The following data is part of a premarket notification filed by Indus Medicare Ltd. with the FDA for Invigra Male Latex Condom Blue Colored And Vanilla Flavored.
Device ID | K000040 |
510k Number | K000040 |
Device Name: | INVIGRA MALE LATEX CONDOM BLUE COLORED AND VANILLA FLAVORED |
Classification | Condom |
Applicant | INDUS MEDICARE LTD. 144, S.P. RD., BEGUMPET Hyderabad Andhra Pradesh, IN 500 016 |
Contact | P.k. Reddy |
Correspondent | P.k. Reddy INDUS MEDICARE LTD. 144, S.P. RD., BEGUMPET Hyderabad Andhra Pradesh, IN 500 016 |
Product Code | HIS |
CFR Regulation Number | 884.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-01-06 |
Decision Date | 2000-03-21 |