Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BROWNE MVI STEAM INDICATOR

K-Number: K971369 · 1998-01-29

Decision Date1998-01-29
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE MVI STEAM INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Albert Browne , Ltd.. It received FDA 510(k) clearance on 1998-01-29 under 510(k) number K971369. 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 MVI STEAM INDICATOR?

BROWNE MVI STEAM INDICATOR is a medical device that received FDA 510(k) clearance on 1998-01-29. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K971369.

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

BROWNE MVI STEAM INDICATOR received FDA 510(k) clearance on 1998-01-29, under 510(k) number K971369.

Who is the listed applicant for BROWNE MVI STEAM INDICATOR?

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

What is the FDA product code for BROWNE MVI STEAM INDICATOR?

The FDA product code for BROWNE MVI STEAM INDICATOR is JOJ.

Related Clinical Trials

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.

Other records listing 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.

View all 19 devices →

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.

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.

↑