FDA 510(k)

GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT

K-Number: K864056 · 1986-10-31

Decision Date1986-10-31

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K864056. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT?

GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Grieshaber & Co.. The 510(k) number is K864056.

When did GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT receive FDA 510(k) clearance?

GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT received FDA 510(k) clearance on 1986-10-31, under 510(k) number K864056.

Who is the listed applicant for GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT?

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 SYSTEM/PRESSURE OPHTHALMIC IRRIGANT?

The FDA product code for GRIESHABER AIR SYSTEM/PRESSURE OPHTHALMIC IRRIGANT is HQC.

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Other records listing Grieshaber & Co. as applicant

K950056THE GRIESHABER AXIAL CUTTER K930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGE K914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGE K914587GRIESHABER AIR/FLUID TUBING SET K914586GRIESHABER THREE FUNCTION MANIPULATOR K914585GRIESHABER TWO FUNCTION MANIPULATOR

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Related Devices (Code: HQC)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.