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FDA 510(k)

GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)

K-Number: K890782 · 1989-06-23

ApplicantGrieshaber & Co.
Decision Date1989-06-23
Product CodeHMX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES) is the device name listed in this FDA 510(k) record. The listed applicant is Grieshaber & Co.. It received FDA 510(k) clearance on 1989-06-23 under 510(k) number K890782. The device is classified under product code HMX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)?

GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES) is a medical device that received FDA 510(k) clearance on 1989-06-23. The listed applicant is Grieshaber & Co.. The 510(k) number is K890782.

When did GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES) receive FDA 510(k) clearance?

GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES) received FDA 510(k) clearance on 1989-06-23, under 510(k) number K890782.

Who is the listed applicant for GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES)?

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 SOFT TIP NEEDLE (20 & 19 GAUGES)?

The FDA product code for GRIESHABER SOFT TIP NEEDLE (20 & 19 GAUGES) is HMX.

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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 SETK914586GRIESHABER THREE FUNCTION MANIPULATORK914585GRIESHABER TWO FUNCTION MANIPULATOR

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Related Devices (Code: HMX)

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.

K010305WEISS RETINAL CANNULAMicron Surgical, Inc.K000457VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIESRetinalabs.ComK970873ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.)American Medical Devices, Inc.K943932STERISEAL OPHTHALMIC CANNULAPharma-Plast, Ltd.K942403INFUSION CANNULAMicrosurgical Technology, Inc.K934844INTER TIP TMicrosurgical Technology, 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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