Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K872504Substantially Equivalent

Lubricated Condom

Royal American Industries, Inc., Boca Raton FL / Traditional, Substantially Equivalent

K872504 is the FDA 510(k) clearance record for LUBRICATED CONDOM, a class II device, cleared for Royal American Industries, Inc. on under FDA product code HIS (Condom). FDA records list 2 510(k) clearances for Royal American Industries, Inc. As of , FDA records show no recalls naming K872504.

Clearance record

Decision date
Received
(149 days to decision)
Product code
HIS Condom
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Royal American Industries, Inc. 10309 Silver Lake Dr., Boca Raton FL
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