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FDA 510(k)

JUZO-RESPIRA ANTI-EMBOLISM STOCKING

K-Number: K905413 · 1991-05-17

Decision Date1991-05-17
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

JUZO-RESPIRA ANTI-EMBOLISM STOCKING is the device name listed in this FDA 510(k) record. The listed applicant is Julius Zorn, Inc.. It received FDA 510(k) clearance on 1991-05-17 under 510(k) number K905413. The device is classified under product code DWL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JUZO-RESPIRA ANTI-EMBOLISM STOCKING?

JUZO-RESPIRA ANTI-EMBOLISM STOCKING is a medical device that received FDA 510(k) clearance on 1991-05-17. The listed applicant is Julius Zorn, Inc.. The 510(k) number is K905413.

When did JUZO-RESPIRA ANTI-EMBOLISM STOCKING receive FDA 510(k) clearance?

JUZO-RESPIRA ANTI-EMBOLISM STOCKING received FDA 510(k) clearance on 1991-05-17, under 510(k) number K905413.

Who is the listed applicant for JUZO-RESPIRA ANTI-EMBOLISM STOCKING?

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

What is the FDA product code for JUZO-RESPIRA ANTI-EMBOLISM STOCKING?

The FDA product code for JUZO-RESPIRA ANTI-EMBOLISM STOCKING is DWL.

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 Julius Zorn, 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: DWL)

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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