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FDA 510(k)

G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY

K-Number: K960146 · 1996-02-27

ApplicantGE Medical Systems
Decision Date1996-02-27
Product CodeIZG
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems. It received FDA 510(k) clearance on 1996-02-27 under 510(k) number K960146. The device is classified under product code IZG. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY?

G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY is a medical device that received FDA 510(k) clearance on 1996-02-27. The listed applicant is GE Medical Systems. The 510(k) number is K960146.

When did G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY receive FDA 510(k) clearance?

G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY received FDA 510(k) clearance on 1996-02-27, under 510(k) number K960146.

Who is the listed applicant for G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY?

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

What is the FDA product code for G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY?

The FDA product code for G.E. STERILE DISPOSABLE RADIOGRAPHIC CONTRAST TRAY is IZG.

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Other records listing GE Medical Systems 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.

K253808AIR Recon DLK220848Venue FitK220851VenueK173341Vivid E80, Vivid E90, Vivid E95K103411IDEAL IQ SOFTWARE OPTIONK073138CARDIQ EXPRESS VERSION 2.0

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Related Devices (Code: IZG)

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.

K960082DISCOGRAPHY KITSpinal Specialties, Inc.K913436PXI PNEUMATIC COMPRESSION PADDLEBrotherston/PxiK920393MU125M MOBILE X-RAY SYSTEMShimadzu Medical SystemsK910503DISCOGRAPHY KITB. Braun of America, Inc.K903808AMSIS RDS, RADIOGRAPHIC DISCOGRAPHY KITAdvanced Med/Surg, Inc.K892659ELECTRODELCAOldelft Corp. of America

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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