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FDA 510(k)

V/P AND L/P CATHETER PASSERS

K-Number: K934391 · 1993-11-19

ApplicantRadionics, Inc.
Decision Date1993-11-19
Product CodeGYK
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

V/P AND L/P CATHETER PASSERS is the device name listed in this FDA 510(k) record. The listed applicant is Radionics, Inc.. It received FDA 510(k) clearance on 1993-11-19 under 510(k) number K934391. The device is classified under product code GYK. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V/P AND L/P CATHETER PASSERS?

V/P AND L/P CATHETER PASSERS is a medical device that received FDA 510(k) clearance on 1993-11-19. The listed applicant is Radionics, Inc.. The 510(k) number is K934391.

When did V/P AND L/P CATHETER PASSERS receive FDA 510(k) clearance?

V/P AND L/P CATHETER PASSERS received FDA 510(k) clearance on 1993-11-19, under 510(k) number K934391.

Who is the listed applicant for V/P AND L/P CATHETER PASSERS?

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

What is the FDA product code for V/P AND L/P CATHETER PASSERS?

The FDA product code for V/P AND L/P CATHETER PASSERS is GYK.

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Related Devices (Code: GYK)

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K962761REIGEL TUNNELING DEVICECook, Inc.K930606PS MEDICAL DISPOSABLE SUBCUTANEOUS CATH PASSERPudenz-Schulte Medical Research Corp.K932273CORDIS TUNNELERCordis Corp.K895868HEYER-SCHULTE DISPOSABLE PERITONEAL CATHETER PASSEBaxter Healthcare CorpK883607PEEL-AWAY INTRODUCER FOR VENTRICULAR CATHETERCodman & Shurtleff, Inc.K873771HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTROAmerican V. Mueller

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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