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FDA 510(k)

THE GRIESHABER AXIAL CUTTER

K-Number: K950056 · 1995-05-05

ApplicantGrieshaber & Co.
Decision Date1995-05-05
Product CodeHKP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE GRIESHABER AXIAL CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1995-05-05 under 510(k) number K950056. The device is classified under product code HKP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE GRIESHABER AXIAL CUTTER?

THE GRIESHABER AXIAL CUTTER is a medical device that received FDA 510(k) clearance on 1995-05-05. The listed applicant is Grieshaber & Co.. The 510(k) number is K950056.

When did THE GRIESHABER AXIAL CUTTER receive FDA 510(k) clearance?

THE GRIESHABER AXIAL CUTTER received FDA 510(k) clearance on 1995-05-05, under 510(k) number K950056.

Who is the listed applicant for THE GRIESHABER AXIAL CUTTER?

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 THE GRIESHABER AXIAL CUTTER?

The FDA product code for THE GRIESHABER AXIAL CUTTER is HKP.

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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.

K930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEK914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEK914587GRIESHABER AIR/FLUID TUBING SETK914585GRIESHABER TWO FUNCTION MANIPULATORK914586GRIESHABER THREE FUNCTION MANIPULATORK897119GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

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Related Devices (Code: HKP)

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.

K952558AARON VAC 2Aaron Medical IndustriesK950287UNIVIT PROBEMedical Instrument Development Laboratories, Inc.K896622VISITEC VITRECTOMY UNITVisitec Co.K890595MENTOR ANTERIOR SEGMENT VITRECTORMentor O & O, Inc.K832074CAVITRON/KELMAN PHACO-EMULSIFIER ASPIRACooperVision, Inc.K822599KEATES I/A SYSTEM FRIGITRONICS 4000Frigitronics of Connecticut, 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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