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FDA 510(k)

NEVOSCOPE

K-Number: K954943 · 1996-03-27

ApplicantNizar A. Mullani
Decision Date1996-03-27
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEVOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Nizar A. Mullani. It received FDA 510(k) clearance on 1996-03-27 under 510(k) number K954943. The device is classified under product code KZF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEVOSCOPE?

NEVOSCOPE is a medical device that received FDA 510(k) clearance on 1996-03-27. The listed applicant is Nizar A. Mullani. The 510(k) number is K954943.

When did NEVOSCOPE receive FDA 510(k) clearance?

NEVOSCOPE received FDA 510(k) clearance on 1996-03-27, under 510(k) number K954943.

Who is the listed applicant for NEVOSCOPE?

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

What is the FDA product code for NEVOSCOPE?

The FDA product code for NEVOSCOPE is KZF.

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Related Devices (Code: KZF)

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.

K952835WELCH ALLYN VIDEO EPISCOPEWelch Allyn, Inc.K945507H 5100, H 5200, H 5300Rudolf Riester GmbH & Co. KGK941869SPLINT, PNEUMATIC, ARM & SPLINT, PNEUMATIC, LEGThe Lighthouse For the Blind, Inc.K936088WAVE FLUORESCENT MAGNIFIERBurton Medical Products Corp.K940284MEDDEV MULTARRAY MEDICAL EXAMINING LIGHT MODIFICATIONMeddev International Corp.K933564SKYTRON EXAM LIGHTSkytron, Div. the Kmw Group, Inc.

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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