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FDA 510(k)

DAVOL KNOT PUSHER

K-Number: K924592 · 1992-12-17

ApplicantDavol, Inc.
Decision Date1992-12-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVOL KNOT PUSHER is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K924592. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL KNOT PUSHER?

DAVOL KNOT PUSHER is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Davol, Inc.. The 510(k) number is K924592.

When did DAVOL KNOT PUSHER receive FDA 510(k) clearance?

DAVOL KNOT PUSHER received FDA 510(k) clearance on 1992-12-17, under 510(k) number K924592.

Who is the listed applicant for DAVOL KNOT PUSHER?

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 KNOT PUSHER?

The FDA product code for DAVOL KNOT PUSHER is GCJ.

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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: GCJ)

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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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