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FDA 510(k)

GRIESHABER AIR/FLUID TUBING SET

K-Number: K914587 · 1992-01-23

ApplicantGrieshaber & Co.
Decision Date1992-01-23
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRIESHABER AIR/FLUID TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1992-01-23 under 510(k) number K914587. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER AIR/FLUID TUBING SET?

GRIESHABER AIR/FLUID TUBING SET is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Grieshaber & Co.. The 510(k) number is K914587.

When did GRIESHABER AIR/FLUID TUBING SET receive FDA 510(k) clearance?

GRIESHABER AIR/FLUID TUBING SET received FDA 510(k) clearance on 1992-01-23, under 510(k) number K914587.

Who is the listed applicant for GRIESHABER AIR/FLUID TUBING SET?

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 AIR/FLUID TUBING SET?

The FDA product code for GRIESHABER AIR/FLUID TUBING SET is KYG.

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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 CARTRIDGEK914585GRIESHABER TWO FUNCTION MANIPULATORK914586GRIESHABER THREE FUNCTION MANIPULATORK897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

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Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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