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FDA 510(k)

DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER

K-Number: K912556 · 1991-09-09

ApplicantDavis & Geck, Inc.
Decision Date1991-09-09
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1991-09-09 under 510(k) number K912556. 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 DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER?

DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER is a medical device that received FDA 510(k) clearance on 1991-09-09. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K912556.

When did DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER receive FDA 510(k) clearance?

DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER received FDA 510(k) clearance on 1991-09-09, under 510(k) number K912556.

Who is the listed applicant for DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER?

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

What is the FDA product code for DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER?

The FDA product code for DAVIS AND GECK LAPRO-LOOP LIGATURE CARRIER is GCJ.

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Related Devices (Code: GCJ)

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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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