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FDA 510(k)

GRIESHABER TWO FUNCTION MANIPULATOR

K-Number: K914585 · 1992-01-03

ApplicantGrieshaber & Co.
Decision Date1992-01-03
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

GRIESHABER TWO FUNCTION MANIPULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1992-01-03 under 510(k) number K914585. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER TWO FUNCTION MANIPULATOR?

GRIESHABER TWO FUNCTION MANIPULATOR is a medical device that received FDA 510(k) clearance on 1992-01-03. The listed applicant is Grieshaber & Co.. The 510(k) number is K914585.

When did GRIESHABER TWO FUNCTION MANIPULATOR receive FDA 510(k) clearance?

GRIESHABER TWO FUNCTION MANIPULATOR received FDA 510(k) clearance on 1992-01-03, under 510(k) number K914585.

Who is the listed applicant for GRIESHABER TWO FUNCTION MANIPULATOR?

The FDA 510(k) record lists Grieshaber & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GRIESHABER TWO FUNCTION MANIPULATOR?

The FDA product code for GRIESHABER TWO FUNCTION MANIPULATOR is EQH.

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Other records listing Grieshaber & Co. 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.

K950056THE GRIESHABER AXIAL CUTTERK930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEK914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEK914587GRIESHABER AIR/FLUID TUBING SETK914586GRIESHABER THREE FUNCTION MANIPULATORK897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

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Related Devices (Code: EQH)

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.

K945876WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHTWells Johnson Co.K954184JED-LIGHT FIBEROPTIC LIGHT SOURCEJedmed Instrument Co.K951829COLD LIGHT SOURCE LOS 150Laser-Optik-Systeme GmbH & Co. KGK932771BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCEXomed-Treace, Inc.K941661GM OPTI*CAM CAMER WITH DENTAL FIBER OPTIC LIGHTGm Engineering, Inc.K941662GM OPTI*CAM CAMERA WITH ENT FIBER OPTIC LIGHTGm Engineering, 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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