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FDA 510(k)

LIC INSTRUMENT PROCESSING SYSTEM

K-Number: K101158 · 2011-05-06

ApplicantLangford IC Systems, Inc.
Decision Date2011-05-06
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LIC INSTRUMENT PROCESSING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Langford IC Systems, Inc.. It received FDA 510(k) clearance on 2011-05-06 under 510(k) number K101158. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIC INSTRUMENT PROCESSING SYSTEM?

LIC INSTRUMENT PROCESSING SYSTEM is a medical device that received FDA 510(k) clearance on 2011-05-06. The listed applicant is Langford IC Systems, Inc.. The 510(k) number is K101158.

When did LIC INSTRUMENT PROCESSING SYSTEM receive FDA 510(k) clearance?

LIC INSTRUMENT PROCESSING SYSTEM received FDA 510(k) clearance on 2011-05-06, under 510(k) number K101158.

Who is the listed applicant for LIC INSTRUMENT PROCESSING SYSTEM?

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

What is the FDA product code for LIC INSTRUMENT PROCESSING SYSTEM?

The FDA product code for LIC INSTRUMENT PROCESSING SYSTEM is FEB.

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 Langford IC Systems, 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.

K060458MANZI MACH 1 INSTRUMENT CLEANER-PROCESSOR SYSTEM, MANZI DETERGENT MD10, MANZI STERILANT MS10, MANZI CHEMICAL INDICATORK043314MANZI CLEANER SYSTEM

Related Devices (Code: FEB)

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.

K241168System 83 Revolve Endoscope Washer/DisinfectorWassenburg Medical, Inc.K243433enspire 3000 Cleaning and Liquid Chemical Sterilant Processing SystemSTERIS CorporationK230930enspire 3000 Cleaning and Liquid Chemical Sterile Processing SystemSTERIS CorporationK213833SCOPE BUDDY PLUS Endoscope Flushing AidMedivators, Inc.K201920Endoscope Reprocessor OER-EliteOlympus Medical Systems Corp.K173590System 83 Plus Washer/DisinfectorCustom Ultrasonics, Inc.

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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