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FDA 510(k)

DEXIDE INSUFFLATION TUBING WITH FILTER

K-Number: K944509 · 1995-02-07

ApplicantDexide, Inc.
Decision Date1995-02-07
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DEXIDE INSUFFLATION TUBING WITH FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Dexide, Inc.. It received FDA 510(k) clearance on 1995-02-07 under 510(k) number K944509. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIDE INSUFFLATION TUBING WITH FILTER?

DEXIDE INSUFFLATION TUBING WITH FILTER is a medical device that received FDA 510(k) clearance on 1995-02-07. The listed applicant is Dexide, Inc.. The 510(k) number is K944509.

When did DEXIDE INSUFFLATION TUBING WITH FILTER receive FDA 510(k) clearance?

DEXIDE INSUFFLATION TUBING WITH FILTER received FDA 510(k) clearance on 1995-02-07, under 510(k) number K944509.

Who is the listed applicant for DEXIDE INSUFFLATION TUBING WITH FILTER?

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

What is the FDA product code for DEXIDE INSUFFLATION TUBING WITH FILTER?

The FDA product code for DEXIDE INSUFFLATION TUBING WITH FILTER is HIF.

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Other records listing Dexide, Inc. as applicant

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Related Devices (Code: HIF)

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K260209ENDOFLATOR+; Smart Smoke EvacuationKarl Storz SE & CO. KGK252584Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)Weyo Surgical Technology , Ltd.K252318Insufflator (OPTO-IFL1000)Guangdong Optomedic Technologies, Inc.K250388ENDOFLATOR +Karl Storz SE & CO. KGK242772AirSurgN Insufflator (10030/AirSurgN)SmartsurgN, Inc.K243527High Flow Insufflation Unit (UHI-4)Olympus Medical Systems Corporation

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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