510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K103119Substantially Equivalent

Billy Boy Male Latex Condom

Sheila Pickering PHD, Los Altos CA / Traditional, Substantially Equivalent

K103119 is the FDA 510(k) clearance record for BILLY BOY MALE LATEX CONDOM, a class II device, cleared for Sheila Pickering PHD on under FDA product code HIS (Condom). FDA records list one 510(k) clearance for Sheila Pickering PHD. As of , FDA records show no recalls naming K103119.

Clearance record

Decision date
Received
(125 days to decision)
Product code
HIS Condom
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Sheila Pickering PHD 2061 Longden Cir., Los Altos CA
510(k) summary
Summary PDF
Third party review
Yes

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