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FDA 510(k)

G.E. STERILE CT BIOPSY TRAY

K-Number: K960144 · 1996-04-15

ApplicantGE Medical Systems
Decision Date1996-04-15
Product CodeDWS
Advisory CommitteeCV
DecisionUnknown

Device Summary

G.E. STERILE CT BIOPSY 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 1996-04-15 under 510(k) number K960144. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the G.E. STERILE CT BIOPSY TRAY?

G.E. STERILE CT BIOPSY TRAY is a medical device that received FDA 510(k) clearance on 1996-04-15. The listed applicant is GE Medical Systems. The 510(k) number is K960144.

When did G.E. STERILE CT BIOPSY TRAY receive FDA 510(k) clearance?

G.E. STERILE CT BIOPSY TRAY received FDA 510(k) clearance on 1996-04-15, under 510(k) number K960144.

Who is the listed applicant for G.E. STERILE CT BIOPSY 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 CT BIOPSY TRAY?

The FDA product code for G.E. STERILE CT BIOPSY TRAY is DWS.

Related Clinical Trials

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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: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960143G.E. STERILE DIGITAL ANGIOGRAPHIC TRAYGE Medical Systems

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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