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FDA 510(k)

HIFLO FILTERED INSUFFLATION TUBING

K-Number: K930508 · 1993-06-25

ApplicantW. J. Medical Instruments, Inc.
Decision Date1993-06-25
Product CodeFCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HIFLO FILTERED INSUFFLATION TUBING is the device name listed in this FDA 510(k) record. The listed applicant is W. J. Medical Instruments, Inc.. It received FDA 510(k) clearance on 1993-06-25 under 510(k) number K930508. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIFLO FILTERED INSUFFLATION TUBING?

HIFLO FILTERED INSUFFLATION TUBING is a medical device that received FDA 510(k) clearance on 1993-06-25. The listed applicant is W. J. Medical Instruments, Inc.. The 510(k) number is K930508.

When did HIFLO FILTERED INSUFFLATION TUBING receive FDA 510(k) clearance?

HIFLO FILTERED INSUFFLATION TUBING received FDA 510(k) clearance on 1993-06-25, under 510(k) number K930508.

Who is the listed applicant for HIFLO FILTERED INSUFFLATION TUBING?

The FDA 510(k) record lists W. J. Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HIFLO FILTERED INSUFFLATION TUBING?

The FDA product code for HIFLO FILTERED INSUFFLATION TUBING is FCX.

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Other records listing W. J. Medical Instruments, 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.

K935947HI-TOPS ELECTRODES 14-8000K930511STEALTH SURGICAL IRRIGATOR ASPIRATOR

Related Devices (Code: FCX)

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.

K262152VS-370CF, VS-370CTVISION MEDICAL Co., Ltd.K240847MedicCO2LON (MedicCO2LON)Ide Vision, Ltd.K230474EVA5 InsufflatorPalliare , Ltd.K202922END 200 Endoscopic TubesetPalliare , Ltd.K201096CO2mbiLEDKarl Storz Endoscopy America, Inc.K190985BAROnova Insufflation System, BAROnova Accessory KitBaronova, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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