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FDA 510(k)

FLUID ASPIRATION NEEDLE

K-Number: K935293 · 1994-02-15

ApplicantSurgin Surgical Instrumentation, Inc.
Decision Date1994-02-15
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLUID ASPIRATION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Surgin Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1994-02-15 under 510(k) number K935293. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLUID ASPIRATION NEEDLE?

FLUID ASPIRATION NEEDLE is a medical device that received FDA 510(k) clearance on 1994-02-15. The listed applicant is Surgin Surgical Instrumentation, Inc.. The 510(k) number is K935293.

When did FLUID ASPIRATION NEEDLE receive FDA 510(k) clearance?

FLUID ASPIRATION NEEDLE received FDA 510(k) clearance on 1994-02-15, under 510(k) number K935293.

Who is the listed applicant for FLUID ASPIRATION NEEDLE?

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

What is the FDA product code for FLUID ASPIRATION NEEDLE?

The FDA product code for FLUID ASPIRATION NEEDLE is GCJ.

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Other records listing Surgin 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.

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Related Devices (Code: GCJ)

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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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