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FDA 510(k)

SUPER-FLOW TUBING

K-Number: K922245 · 1993-09-03

ApplicantArmm, Inc.
Decision Date1993-09-03
Product CodeHIF
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUPER-FLOW TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Armm, Inc.. It received FDA 510(k) clearance on 1993-09-03 under 510(k) number K922245. 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 SUPER-FLOW TUBING?

SUPER-FLOW TUBING is a medical device that received FDA 510(k) clearance on 1993-09-03. The listed applicant is Armm, Inc.. The 510(k) number is K922245.

When did SUPER-FLOW TUBING receive FDA 510(k) clearance?

SUPER-FLOW TUBING received FDA 510(k) clearance on 1993-09-03, under 510(k) number K922245.

Who is the listed applicant for SUPER-FLOW TUBING?

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

What is the FDA product code for SUPER-FLOW TUBING?

The FDA product code for SUPER-FLOW TUBING is HIF.

Related Clinical Trials

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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Other records listing Armm, 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.

K981286SUPERFLOW IRRIGATION AND ASPIRATION TUBING SETSK923201ENDOSI SUCTION IRRIGATORK931607MEDDRAINS

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

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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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