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FDA 510(k)

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE

K-Number: K930842 · 1994-05-03

ApplicantGrieshaber & Co.
Decision Date1994-05-03
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1994-05-03 under 510(k) number K930842. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE?

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE is a medical device that received FDA 510(k) clearance on 1994-05-03. The listed applicant is Grieshaber & Co.. The 510(k) number is K930842.

When did THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE receive FDA 510(k) clearance?

THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE received FDA 510(k) clearance on 1994-05-03, under 510(k) number K930842.

Who is the listed applicant for THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE?

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 SYST/AI TUBING SET AND CARTRIDGE?

The FDA product code for THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE is HQE.

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Other records listing Grieshaber & Co. as applicant

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K950056THE GRIESHABER AXIAL CUTTERK914588GRIESHABER 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: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, 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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