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FDA 510(k)

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE

K-Number: K884043 · 1988-11-16

ApplicantGrieshaber & Co.
Decision Date1988-11-16
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1988-11-16 under 510(k) number K884043. 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 GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE?

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE is a medical device that received FDA 510(k) clearance on 1988-11-16. The listed applicant is Grieshaber & Co.. The 510(k) number is K884043.

When did GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE receive FDA 510(k) clearance?

GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE received FDA 510(k) clearance on 1988-11-16, under 510(k) number K884043.

Who is the listed applicant for GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE?

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 MICRO LITE LIGHT PIPE 19 & 20 GAUGE?

The FDA product code for GRIESHABER MICRO LITE LIGHT PIPE 19 & 20 GAUGE is HQE.

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Other records listing Grieshaber & Co. as applicant

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K950056THE GRIESHABER AXIAL CUTTERK930842THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEK914588GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEK914587GRIESHABER AIR/FLUID TUBING SETK914586GRIESHABER THREE FUNCTION MANIPULATORK914585GRIESHABER TWO FUNCTION MANIPULATOR

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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.

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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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