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FDA 510(k)

DANESHVAR WOUND SUPPORT UNIT

K-Number: K955827 · 1996-10-02

ApplicantY. Daneshvar
Decision Date1996-10-02
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DANESHVAR WOUND SUPPORT UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Y. Daneshvar. It received FDA 510(k) clearance on 1996-10-02 under 510(k) number K955827. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANESHVAR WOUND SUPPORT UNIT?

DANESHVAR WOUND SUPPORT UNIT is a medical device that received FDA 510(k) clearance on 1996-10-02. The listed applicant is Y. Daneshvar. The 510(k) number is K955827.

When did DANESHVAR WOUND SUPPORT UNIT receive FDA 510(k) clearance?

DANESHVAR WOUND SUPPORT UNIT received FDA 510(k) clearance on 1996-10-02, under 510(k) number K955827.

Who is the listed applicant for DANESHVAR WOUND SUPPORT UNIT?

The FDA 510(k) record lists Y. Daneshvar as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DANESHVAR WOUND SUPPORT UNIT?

The FDA product code for DANESHVAR WOUND SUPPORT UNIT is DXC.

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 Y. Daneshvar 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: DXC)

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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