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FDA 510(k)

BROWNE STEAM INDICATOR

K-Number: K970918 · 1997-06-24

ApplicantBoard of Directors, Albert Browne , Ltd.
Decision Date1997-06-24
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE STEAM INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Board of Directors, Albert Browne , Ltd.. It received FDA 510(k) clearance on 1997-06-24 under 510(k) number K970918. 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 STEAM INDICATOR?

BROWNE STEAM INDICATOR is a medical device that received FDA 510(k) clearance on 1997-06-24. The listed applicant is Board of Directors, Albert Browne , Ltd.. The 510(k) number is K970918.

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

BROWNE STEAM INDICATOR received FDA 510(k) clearance on 1997-06-24, under 510(k) number K970918.

Who is the listed applicant for BROWNE STEAM INDICATOR?

The FDA 510(k) record lists Board of Directors, Albert Browne , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BROWNE STEAM INDICATOR?

The FDA product code for BROWNE STEAM INDICATOR is JOJ.

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Other records listing Board of Directors, Albert Browne , Ltd. as applicant

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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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

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

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