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FDA 510(k), K030176, LIFESTYLES, CONTEMPO OR PRIVATE LABEL-MALE LATEX CONDOM WITH DESENSITIZING LUBRICANT
FDA 510(k), K030176, LIFESTYLES, CONTEMPO OR PRIVATE LABEL-MALE LATEX CONDOM WITH DESENSITIZING LUBRICANT
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510(K) Number: K030176
Device Name: LIFESTYLES, CONTEMPO OR PRIVATE LABEL-MALE LATEX CONDOM WITH DESENSITIZING LUBRICANT
Manufacturer: SURETEX, LTD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 01/17/2003
Decision Date: 04/17/2003
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: LIFESTYLES, CONTEMPO OR PRIVATE LABEL-MALE LATEX CONDOM WITH DESENSITIZING LUBRICANT
Manufacturer: SURETEX, LTD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 01/17/2003
Decision Date: 04/17/2003
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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