510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K920838Substantially Equivalent

Medsurg Circumcision Tray

Medsurg Industries, Inc., Herndon VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K920838 is the FDA 510(k) clearance record for MEDSURG CIRCUMCISION TRAY, a class II device, cleared for Medsurg Industries, Inc. on under FDA product code HFK (Mold, Vaginal). FDA records list 41 510(k) clearances for Medsurg Industries, Inc., from to . As of , FDA records show no recalls naming K920838.

Clearance record

Decision date
Received
(599 days to decision)
Product code
HFK Mold, Vaginal
Regulation
21 CFR 884.3900
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Medsurg Industries, Inc. 251 Exchange Pl., Herndon VA
510(k) summary
Statement
Third party review
No

Clearances, product code HFK

Trailing 12 months

FDA records hold no clearances under product code HFK in the trailing twelve months.

FDA records show no clearances under product code HFK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HFK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260