510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K946207Substantially Equivalent

Conqueror, Rumba and Temptation

Frontline Latex Products Pvt., Ltd., New York NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K946207 is the FDA 510(k) clearance record for CONQUEROR, RUMBA AND TEMPTATION, a class II device, cleared for Frontline Latex Products Pvt. , Ltd. on under FDA product code HIS (Condom). FDA records list 2 510(k) clearances for Frontline Latex Products Pvt. , Ltd., from to . As of , FDA records show no recalls naming K946207.

Clearance record

Decision date
Received
(399 days to decision)
Product code
HIS Condom
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Frontline Latex Products Pvt. , Ltd. 57 W. 38th St., New York NY
510(k) summary
Statement
Third party review
No

Clearances, product code HIS

Trailing 12 months
3 clearances under product code HIS in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HIS, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260