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FDA 510(k)

DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT

K-Number: K914755 · 1992-03-30

ApplicantDavol, Inc.
Decision Date1992-03-30
Product CodeGCA
Advisory CommitteeGU
DecisionUnknown

Device Summary

DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1992-03-30 under 510(k) number K914755. The device is classified under product code GCA. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT?

DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT is a medical device that received FDA 510(k) clearance on 1992-03-30. The listed applicant is Davol, Inc.. The 510(k) number is K914755.

When did DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT receive FDA 510(k) clearance?

DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT received FDA 510(k) clearance on 1992-03-30, under 510(k) number K914755.

Who is the listed applicant for DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT?

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

What is the FDA product code for DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT?

The FDA product code for DAVOL LAPAROSCOPIC CHOLANGIOGRAM CATHETER & KIT is GCA.

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Other records listing Davol, Inc. as applicant

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K251557Bard® Mesh; Bard® Mesh Pre-ShapedK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedK031213AQUASENS FLUID MONITORING SYSTEMK030307DAVOL ARTHROVENT OUTFLOW TUBINGK003323COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205K003790DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000, 5552001, 552002, 5552003, 5552004, 5552005

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Related Devices (Code: GCA)

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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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