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FDA 510(k)

VENES II

K-Number: K811085 · 1981-05-01

Decision Date1981-05-01
Product CodeDWL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENES II is the device name listed in this FDA 510(k) record. The listed applicant is Jung Products, Inc.. It received FDA 510(k) clearance on 1981-05-01 under 510(k) number K811085. 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 VENES II?

VENES II is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Jung Products, Inc.. The 510(k) number is K811085.

When did VENES II receive FDA 510(k) clearance?

VENES II received FDA 510(k) clearance on 1981-05-01, under 510(k) number K811085.

Who is the listed applicant for VENES II?

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

What is the FDA product code for VENES II?

The FDA product code for VENES II 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 Jung Products, 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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