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FDA 510(k)

VST-10, VST-10/2

K-Number: K960433 · 1996-05-21

ApplicantVcare Intl., Inc.
Decision Date1996-05-21
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent for Some Indications

Device Summary

VST-10, VST-10/2 is the device name listed in this FDA 510(k) record. The listed applicant is Vcare Intl., Inc.. It received FDA 510(k) clearance on 1996-05-21 under 510(k) number K960433. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the VST-10, VST-10/2?

VST-10, VST-10/2 is a medical device that received FDA 510(k) clearance on 1996-05-21. The listed applicant is Vcare Intl., Inc.. The 510(k) number is K960433.

When did VST-10, VST-10/2 receive FDA 510(k) clearance?

VST-10, VST-10/2 received FDA 510(k) clearance on 1996-05-21, under 510(k) number K960433.

Who is the listed applicant for VST-10, VST-10/2?

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

What is the FDA product code for VST-10, VST-10/2?

The FDA product code for VST-10, VST-10/2 is IPF.

Related Devices (Code: IPF)

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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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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