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FDA 510(k)

VITAPEN

K-Number: K924447 · 1993-09-27

ApplicantVitajet Corp.
Decision Date1993-09-27
Product CodeKZF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VITAPEN is the device name listed in this FDA 510(k) record. The listed applicant is Vitajet Corp.. It received FDA 510(k) clearance on 1993-09-27 under 510(k) number K924447. 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 VITAPEN?

VITAPEN is a medical device that received FDA 510(k) clearance on 1993-09-27. The listed applicant is Vitajet Corp.. The 510(k) number is K924447.

When did VITAPEN receive FDA 510(k) clearance?

VITAPEN received FDA 510(k) clearance on 1993-09-27, under 510(k) number K924447.

Who is the listed applicant for VITAPEN?

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

What is the FDA product code for VITAPEN?

The FDA product code for VITAPEN is KZF.

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 Vitajet Corp. 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.

K962625VITAJETK945548MEDIVAX

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.

K954943NEVOSCOPENizar A. MullaniK952835WELCH 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.

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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