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FDA 510(k)

ASPIRATION/IRRIGATION CATHETER

K-Number: K961300 · 1996-06-07

ApplicantNeuro Navigational Corp.
Decision Date1996-06-07
Product CodeGWG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ASPIRATION/IRRIGATION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Navigational Corp.. It received FDA 510(k) clearance on 1996-06-07 under 510(k) number K961300. The device is classified under product code GWG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASPIRATION/IRRIGATION CATHETER?

ASPIRATION/IRRIGATION CATHETER is a medical device that received FDA 510(k) clearance on 1996-06-07. The listed applicant is Neuro Navigational Corp.. The 510(k) number is K961300.

When did ASPIRATION/IRRIGATION CATHETER receive FDA 510(k) clearance?

ASPIRATION/IRRIGATION CATHETER received FDA 510(k) clearance on 1996-06-07, under 510(k) number K961300.

Who is the listed applicant for ASPIRATION/IRRIGATION CATHETER?

The FDA 510(k) record lists Neuro Navigational Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASPIRATION/IRRIGATION CATHETER?

The FDA product code for ASPIRATION/IRRIGATION CATHETER is GWG.

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Other records listing Neuro Navigational Corp. 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.

K9650782.1MM SEMI-RIGID NEUROVIEW SCISSORS/2.0OMM SEMI-RIGID NEUROVIEW GRASPING FORCEPSK961406NEUROVIEW SCISSORSK9611731.2MM REUSABLE NEUROVIEW ENDOSCOPEK960792DISPOSABLE NEUROVIEW INTRODUCER SHEATHK954938DISPOSABLE NEUROVIEW OPERATING SHEATHK955351NEUROVIEW COAXIAL BIPOLAR ELECTRODE

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Related Devices (Code: GWG)

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.

K253602Precision S 4K SinuscopeStryker EndoscopyK253679Hydro Irrigation SystemStryker InstrumentsK243429HJY VisualNext 3D Endoscopic Vision SystemHjy Smart Medical Device Co., Ltd.K250752AURORA® Surgiscope® System (ASX15/60); AURORA® Surgiscope® System (ASX15/80)Integra LifeSciences CorporationK233391cCeLL - In vivoVPIX Medical, Inc.K223615Digital ClarusScope System, Digital NeuroPEN SystemClarus Medical, LLC

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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