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FDA 510(k)

WINDSOR MEDICAL VARIOUS MODELS

K-Number: K832606 · 1983-11-29

Decision Date1983-11-29
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WINDSOR MEDICAL VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Windsor Medical, Inc.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K832606. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WINDSOR MEDICAL VARIOUS MODELS?

WINDSOR MEDICAL VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Windsor Medical, Inc.. The 510(k) number is K832606.

When did WINDSOR MEDICAL VARIOUS MODELS receive FDA 510(k) clearance?

WINDSOR MEDICAL VARIOUS MODELS received FDA 510(k) clearance on 1983-11-29, under 510(k) number K832606.

Who is the listed applicant for WINDSOR MEDICAL VARIOUS MODELS?

The FDA 510(k) record lists Windsor Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WINDSOR MEDICAL VARIOUS MODELS?

The FDA product code for WINDSOR MEDICAL VARIOUS MODELS is FRN.

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 Windsor Medical, Inc. 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 9 devices →

Related Devices (Code: FRN)

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.

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