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FDA 510(k)

MED-LOGICS DISPOSABLE ALK TUBING

K-Number: K010353 · 2001-04-27

ApplicantMed-Logics, Inc.
Decision Date2001-04-27
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MED-LOGICS DISPOSABLE ALK TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Med-Logics, Inc.. It received FDA 510(k) clearance on 2001-04-27 under 510(k) number K010353. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-LOGICS DISPOSABLE ALK TUBING?

MED-LOGICS DISPOSABLE ALK TUBING is a medical device that received FDA 510(k) clearance on 2001-04-27. The listed applicant is Med-Logics, Inc.. The 510(k) number is K010353.

When did MED-LOGICS DISPOSABLE ALK TUBING receive FDA 510(k) clearance?

MED-LOGICS DISPOSABLE ALK TUBING received FDA 510(k) clearance on 2001-04-27, under 510(k) number K010353.

Who is the listed applicant for MED-LOGICS DISPOSABLE ALK TUBING?

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

What is the FDA product code for MED-LOGICS DISPOSABLE ALK TUBING?

The FDA product code for MED-LOGICS DISPOSABLE ALK TUBING is KYG.

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Other records listing Med-Logics, 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.

K033293MED-LOGICS, MODEL ML7090K022982MED-LOGICS MICROKERATOME BLADE, MODEL 7050CLBK022716MED-LOGICS MICROKERATOME BLADE, MODEL 7020CLBK010872ML BLADE, MODEL ML7030K002515MEDLOGICS ML 4000, MODEL 4000K002279ML EYE SPEAR, MODEL ML 27 ES

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Related Devices (Code: KYG)

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.

K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, Inc.K971173ML DISPOSABLE ALK TUBINGMed-Logics, 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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