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FDA 510(k)

SIL-V-UR CHEST CATHETER

K-Number: K813463 · 1982-02-12

ApplicantC.R. Bard, Inc.
Decision Date1982-02-12
Product CodeGBS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SIL-V-UR CHEST CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1982-02-12 under 510(k) number K813463. The device is classified under product code GBS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIL-V-UR CHEST CATHETER?

SIL-V-UR CHEST CATHETER is a medical device that received FDA 510(k) clearance on 1982-02-12. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K813463.

When did SIL-V-UR CHEST CATHETER receive FDA 510(k) clearance?

SIL-V-UR CHEST CATHETER received FDA 510(k) clearance on 1982-02-12, under 510(k) number K813463.

Who is the listed applicant for SIL-V-UR CHEST CATHETER?

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

What is the FDA product code for SIL-V-UR CHEST CATHETER?

The FDA product code for SIL-V-UR CHEST CATHETER is GBS.

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Related Devices (Code: GBS)

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K912645ATRIUMS PDR THORACIC CATHETERAtrium Medical Corp.K883887AXIOM ATRAUM WOUND DRAINSAxiom, Inc.K881873INTRODUCTION/DRAINAGE CATHETER & ACCESSSheridan Catheter Corp.K880895URESIL WOUND DRAIN TROCARUresil Corp.K880376NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAPGenesis Industries, Inc.K873377CLOSED CHEST DRAINAGE SET W/SUTURESGish Biomedical, Inc.

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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