JUZO-RESPIRA ANTI-EMBOLISM STOCKING
K-Number: K905413 · 1991-05-17
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Device Summary
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
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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