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FDA 510(k)

DAVIS & GECK NEEDLE/SHARPS COUNTER

K-Number: K811191 · 1981-05-27

ApplicantDavis & Geck, Inc.
Decision Date1981-05-27
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVIS & GECK NEEDLE/SHARPS COUNTER 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 1981-05-27 under 510(k) number K811191. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVIS & GECK NEEDLE/SHARPS COUNTER?

DAVIS & GECK NEEDLE/SHARPS COUNTER is a medical device that received FDA 510(k) clearance on 1981-05-27. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K811191.

When did DAVIS & GECK NEEDLE/SHARPS COUNTER receive FDA 510(k) clearance?

DAVIS & GECK NEEDLE/SHARPS COUNTER received FDA 510(k) clearance on 1981-05-27, under 510(k) number K811191.

Who is the listed applicant for DAVIS & GECK NEEDLE/SHARPS COUNTER?

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 & GECK NEEDLE/SHARPS COUNTER?

The FDA product code for DAVIS & GECK NEEDLE/SHARPS COUNTER is KDC.

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Other records listing Davis & Geck, Inc. as applicant

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.

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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