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FDA 510(k)

VOXGRAM

K-Number: K954200 · 1995-09-29

ApplicantVoxel
Decision Date1995-09-29
Product CodeIWZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VOXGRAM is the device name listed in this FDA 510(k) record. The listed applicant is Voxel. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K954200. The device is classified under product code IWZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOXGRAM?

VOXGRAM is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Voxel. The 510(k) number is K954200.

When did VOXGRAM receive FDA 510(k) clearance?

VOXGRAM received FDA 510(k) clearance on 1995-09-29, under 510(k) number K954200.

Who is the listed applicant for VOXGRAM?

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

What is the FDA product code for VOXGRAM?

The FDA product code for VOXGRAM is IWZ.

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 Voxel 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.

K954199VOXBOXK954198VOXCAM

Related Devices (Code: IWZ)

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.

K970154KODAK EKTASIAN HG FILM (EHG-15)Eastman Kodak CompanyK9316043M MEDICAL DIAGNOSTIC VIDEOCASSETTE3M Health Care, Ltd.K9316053M MEDICAL DIAGNOSTIC SUPER VHS VIDEOCASSETTE3M Health Care, Ltd.K920539ORWO X-RAY FILMBurkhart Roentgen Intl., Inc.K884827KODAK DENTAL BARRIER PACEastman Kodak CompanyK862944KODAK CFT FILM SO-141Eastman Kodak Company

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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