VENES ANTI EMBOLISM STOCKINGS
K-Number: K830696 · 1983-03-31
Advertisement
Device Summary
Frequently Asked Questions
What is the VENES ANTI EMBOLISM STOCKINGS?
VENES ANTI EMBOLISM STOCKINGS is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Futuro Div. Jung Corp.. The 510(k) number is K830696.
When did VENES ANTI EMBOLISM STOCKINGS receive FDA 510(k) clearance?
VENES ANTI EMBOLISM STOCKINGS received FDA 510(k) clearance on 1983-03-31, under 510(k) number K830696.
Who is the listed applicant for VENES ANTI EMBOLISM STOCKINGS?
The FDA 510(k) record lists Futuro Div. Jung Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENES ANTI EMBOLISM STOCKINGS?
The FDA product code for VENES ANTI EMBOLISM STOCKINGS 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 Futuro Div. Jung Corp. 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.
Advertisement