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FDA 510(k)

G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY

K-Number: K960204 · 1996-02-27

ApplicantGE Medical Systems
Decision Date1996-02-27
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC 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 K960204. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY?

G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC 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 K960204.

When did G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY receive FDA 510(k) clearance?

G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY received FDA 510(k) clearance on 1996-02-27, under 510(k) number K960204.

Who is the listed applicant for G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC 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, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY?

The FDA product code for G.E. STERILE, PERCUTANEOUS CHOLANGIOGRAPHIC TRAY is FRG.

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Related Devices (Code: FRG)

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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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