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FDA 510(k)

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP

K-Number: K897119 · 1990-04-12

ApplicantGrieshaber & Co.
Decision Date1990-04-12
Product CodeHQW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1990-04-12 under 510(k) number K897119. The device is classified under product code HQW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP?

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP is a medical device that received FDA 510(k) clearance on 1990-04-12. The listed applicant is Grieshaber & Co.. The 510(k) number is K897119.

When did GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP receive FDA 510(k) clearance?

GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP received FDA 510(k) clearance on 1990-04-12, under 510(k) number K897119.

Who is the listed applicant for GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP?

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 RETINAL TACK AND SUTHERLAND TACK FORCEP?

The FDA product code for GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEP is HQW.

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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 SETK914585GRIESHABER TWO FUNCTION MANIPULATORK914586GRIESHABER THREE FUNCTION MANIPULATOR

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Related Devices (Code: HQW)

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.

K901275RETINAL TAAKAlcon Surgical, Inc.K840207DOUBLE & SINGLE TANTALUM CLIPSStorz Instrument Co.

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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