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FDA 510(k)

DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES

K-Number: K922526 · 1992-09-02

ApplicantDavol, Inc.
Decision Date1992-09-02
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1992-09-02 under 510(k) number K922526. 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 LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES?

DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES is a medical device that received FDA 510(k) clearance on 1992-09-02. The listed applicant is Davol, Inc.. The 510(k) number is K922526.

When did DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES receive FDA 510(k) clearance?

DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES received FDA 510(k) clearance on 1992-09-02, under 510(k) number K922526.

Who is the listed applicant for DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES?

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 LOOP AND RETRIEVAL DEVICES?

The FDA product code for DAVOL LAPAROSCOPIC LOOP AND RETRIEVAL DEVICES is GCJ.

Related Clinical Trials

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.

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.

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Related Devices (Code: GCJ)

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.

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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