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FDA 510(k)

BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR

K-Number: K120435 · 2012-06-04

ApplicantSTERIS Corporation
Decision Date2012-06-04
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2012-06-04 under 510(k) number K120435. 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 BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR?

BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR is a medical device that received FDA 510(k) clearance on 2012-06-04. The listed applicant is STERIS Corporation. The 510(k) number is K120435.

When did BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR receive FDA 510(k) clearance?

BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR received FDA 510(k) clearance on 2012-06-04, under 510(k) number K120435.

Who is the listed applicant for BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR?

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

What is the FDA product code for BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR?

The FDA product code for BROWNE ALDAHOL GLUTARALDEHYDE INDICATOR is JOJ.

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Related Devices (Code: 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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