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FDA 510(k)

D. DEVICE II

K-Number: K955742 · 1996-08-12

ApplicantYousef Daneshvar
Decision Date1996-08-12
Product CodeDXC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

D. DEVICE II is the device name listed in this FDA 510(k) record. The listed applicant is Yousef Daneshvar. It received FDA 510(k) clearance on 1996-08-12 under 510(k) number K955742. 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 D. DEVICE II?

D. DEVICE II is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is Yousef Daneshvar. The 510(k) number is K955742.

When did D. DEVICE II receive FDA 510(k) clearance?

D. DEVICE II received FDA 510(k) clearance on 1996-08-12, under 510(k) number K955742.

Who is the listed applicant for D. DEVICE II?

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

What is the FDA product code for D. DEVICE II?

The FDA product code for D. DEVICE II is DXC.

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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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