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FDA 510(k)

BROWNE RAPICIDE GLUTARALDEHYDE INDICATOR

K-Number: K080750 · 2008-05-12

ApplicantSTERIS Corporation
Decision Date2008-05-12
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE RAPICIDE 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 2008-05-12 under 510(k) number K080750. 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 RAPICIDE GLUTARALDEHYDE INDICATOR?

BROWNE RAPICIDE GLUTARALDEHYDE INDICATOR is a medical device that received FDA 510(k) clearance on 2008-05-12. The listed applicant is STERIS Corporation. The 510(k) number is K080750.

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

BROWNE RAPICIDE GLUTARALDEHYDE INDICATOR received FDA 510(k) clearance on 2008-05-12, under 510(k) number K080750.

Who is the listed applicant for BROWNE RAPICIDE 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 RAPICIDE GLUTARALDEHYDE INDICATOR?

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

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Related Devices (Code: JOJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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