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FDA 510(k)

INSUFFLATOR CONNECTING FILTER

K-Number: K923194 · 1993-10-08

ApplicantProcedure Products, Inc.
Decision Date1993-10-08
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INSUFFLATOR CONNECTING FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Procedure Products, Inc.. It received FDA 510(k) clearance on 1993-10-08 under 510(k) number K923194. 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 INSUFFLATOR CONNECTING FILTER?

INSUFFLATOR CONNECTING FILTER is a medical device that received FDA 510(k) clearance on 1993-10-08. The listed applicant is Procedure Products, Inc.. The 510(k) number is K923194.

When did INSUFFLATOR CONNECTING FILTER receive FDA 510(k) clearance?

INSUFFLATOR CONNECTING FILTER received FDA 510(k) clearance on 1993-10-08, under 510(k) number K923194.

Who is the listed applicant for INSUFFLATOR CONNECTING FILTER?

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

What is the FDA product code for INSUFFLATOR CONNECTING FILTER?

The FDA product code for INSUFFLATOR CONNECTING FILTER is HIF.

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Other records listing Procedure Products, Inc. as applicant

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Related Devices (Code: HIF)

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.

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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