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FDA 510(k)

ENDPOINT 500 PERACETIC ACID TEST INDICATORS

K-Number: K931935 · 1994-02-07

ApplicantMinntech Corp.
Decision Date1994-02-07
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ENDPOINT 500 PERACETIC ACID TEST INDICATORS is the device name listed in this FDA 510(k) record. The listed applicant is Minntech Corp.. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K931935. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDPOINT 500 PERACETIC ACID TEST INDICATORS?

ENDPOINT 500 PERACETIC ACID TEST INDICATORS is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Minntech Corp.. The 510(k) number is K931935.

When did ENDPOINT 500 PERACETIC ACID TEST INDICATORS receive FDA 510(k) clearance?

ENDPOINT 500 PERACETIC ACID TEST INDICATORS received FDA 510(k) clearance on 1994-02-07, under 510(k) number K931935.

Who is the listed applicant for ENDPOINT 500 PERACETIC ACID TEST INDICATORS?

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 ENDPOINT 500 PERACETIC ACID TEST INDICATORS?

The FDA product code for ENDPOINT 500 PERACETIC ACID TEST INDICATORS is JOJ.

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Official Source

View on FDA Database →

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

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