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FDA 510(k)

ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS

K-Number: K923159 · 1992-08-06

Decision Date1992-08-06
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Arjo-Century, Inc.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K923159. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS?

ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Arjo-Century, Inc.. The 510(k) number is K923159.

When did ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS receive FDA 510(k) clearance?

ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS received FDA 510(k) clearance on 1992-08-06, under 510(k) number K923159.

Who is the listed applicant for ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS?

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

What is the FDA product code for ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS?

The FDA product code for ARJO-CENTURY PODIATRIC WHIRLPOOL SYSTEMS is ILJ.

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 Arjo-Century, 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.

Related Devices (Code: ILJ)

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

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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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