510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960513Substantially Equivalent

Peract 20 Liquid Sterilant

Medivators Inc, Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960513 is the FDA 510(k) clearance record for PERACT 20 LIQUID STERILANT, a class II device, cleared for Minntech Corp. on under FDA product code MED (Sterilant, Medical Devices). FDA records list 46 510(k) clearances for Medivators Inc, from to . As of , FDA records show no recalls naming K960513.

Clearance record

Decision date
Received
(604 days to decision)
Product code
MED Sterilant, Medical Devices
Regulation
21 CFR 880.6885
Device class
Class II
Review panel
General Hospital
Applicant
Minntech Corp. 14605 28th Ave. N., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code MED

Trailing 12 months
1 clearance under product code MED 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 MED, 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