510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K023305Substantially Equivalent

Kegelmaster 2000

Kegelmaster 2000, Ltd., Crofton MD / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K023305 is the FDA 510(k) clearance record for KEGELMASTER 2000, a class II device, cleared for Kegelmaster 2000 , Ltd. on under FDA product code HIR (Perineometer). FDA records list one 510(k) clearance for Kegelmaster 2000 , Ltd. As of , FDA records show no recalls naming K023305.

Clearance record

Decision date
Received
(84 days to decision)
Product code
HIR Perineometer
Regulation
21 CFR 884.1425
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Kegelmaster 2000 , Ltd. P.O. Box 4341, Crofton MD
510(k) summary
Statement
Third party review
No

Clearances, product code HIR

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