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FDA 510(k)

VERRES NEEDLE

K-Number: K932281 · 1993-08-06

ApplicantSurgeon Surgical Instrumentation, Inc.
Decision Date1993-08-06
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VERRES NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Surgeon Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1993-08-06 under 510(k) number K932281. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERRES NEEDLE?

VERRES NEEDLE is a medical device that received FDA 510(k) clearance on 1993-08-06. The listed applicant is Surgeon Surgical Instrumentation, Inc.. The 510(k) number is K932281.

When did VERRES NEEDLE receive FDA 510(k) clearance?

VERRES NEEDLE received FDA 510(k) clearance on 1993-08-06, under 510(k) number K932281.

Who is the listed applicant for VERRES NEEDLE?

The FDA 510(k) record lists Surgeon Surgical Instrumentation, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERRES NEEDLE?

The FDA product code for VERRES NEEDLE is GCT.

Related Clinical Trials

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Other records listing Surgeon Surgical Instrumentation, Inc. 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.

K954241SURGIN GENISIS PHACOEMULSIFIERK922038CO2 INSUFFLATION TUBINGK904010SURGICAL ASPIRATOR KITK890447HEMORRHAGE OCCLUDORK880543UNI-PORTK881232SURGIN EYE SHIELD

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Related Devices (Code: GCT)

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.

K093125ALPHAXENON LIGHT 180 W AND 300 WGimmi GmbHK082925XENON-100 SCB LIGHT SOURCE, MODEL 20132620KARL STORZ Endoscopy-America, Inc.K070376CONMED LINVATEC 300W XENON LIGHT SOURCEConmed LinvatecK040949VIADUCT MINISCOPE AND ACCESSORIESAcueity, Inc.K022490KSEA MEDI PACKKARL STORZ Endoscopy-America, Inc.K031994LINVATEC 300W XENON LIGHT SOURCELinvatec Corp.

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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