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FDA 510(k)

DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE)

K-Number: K914910 · 1992-01-06

ApplicantDavol, Inc.
Decision Date1992-01-06
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE) is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1992-01-06 under 510(k) number K914910. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE)?

DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE) is a medical device that received FDA 510(k) clearance on 1992-01-06. The listed applicant is Davol, Inc.. The 510(k) number is K914910.

When did DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE) receive FDA 510(k) clearance?

DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE) received FDA 510(k) clearance on 1992-01-06, under 510(k) number K914910.

Who is the listed applicant for DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE)?

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 INSTRUMENTS (GEN SURG REUSABLE)?

The FDA product code for DAVOL LAPAROSCOPIC INSTRUMENTS (GEN SURG REUSABLE) is GEI.

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Other records listing Davol, Inc. 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.

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: GEI)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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