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FDA 510(k)

VENES CUSTON RX

K-Number: K820484 · 1982-03-18

ApplicantJung Products, Inc.
Decision Date1982-03-18
Product CodeFQL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VENES CUSTON RX 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 1982-03-18 under 510(k) number K820484. The device is classified under product code FQL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENES CUSTON RX?

VENES CUSTON RX is a medical device that received FDA 510(k) clearance on 1982-03-18. The listed applicant is Jung Products, Inc.. The 510(k) number is K820484.

When did VENES CUSTON RX receive FDA 510(k) clearance?

VENES CUSTON RX received FDA 510(k) clearance on 1982-03-18, under 510(k) number K820484.

Who is the listed applicant for VENES CUSTON RX?

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 CUSTON RX?

The FDA product code for VENES CUSTON RX is FQL.

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.

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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.

K811085VENES II

Related Devices (Code: FQL)

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.

K944240SOFT SOCKSilipos, Inc.K823789ELASTIC COMPRESSION ANKLETOrthopaedic Resources Corp.K823350ELASTIC COMPRESSION ANKLETPodiatry Products Corp.K821260VITOFITSelomas, Inc.K821259VITASANSelomas, Inc.

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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