FDA 510(k)

PERACT 20 LIQUID STERILANT

K-Number: K960513 · 1997-10-01

Decision Date1997-10-01

Product CodeMED

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PERACT 20 LIQUID STERILANT is the device name listed in this FDA 510(k) record. The listed applicant is Minntech Corp.. It received FDA 510(k) clearance on 1997-10-01 under 510(k) number K960513. The device is classified under product code MED. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERACT 20 LIQUID STERILANT?

PERACT 20 LIQUID STERILANT is a medical device that received FDA 510(k) clearance on 1997-10-01. The listed applicant is Minntech Corp.. The 510(k) number is K960513.

When did PERACT 20 LIQUID STERILANT receive FDA 510(k) clearance?

PERACT 20 LIQUID STERILANT received FDA 510(k) clearance on 1997-10-01, under 510(k) number K960513.

Who is the listed applicant for PERACT 20 LIQUID STERILANT?

The FDA 510(k) record lists Minntech Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERACT 20 LIQUID STERILANT?

The FDA product code for PERACT 20 LIQUID STERILANT is MED.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.