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FDA 510(k)

ML UNIVERSAL TUBING

K-Number: K983448 · 1998-12-18

ApplicantMed-Logics, Inc.
Decision Date1998-12-18
Product CodeMSR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ML UNIVERSAL 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 1998-12-18 under 510(k) number K983448. The device is classified under product code MSR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ML UNIVERSAL TUBING?

ML UNIVERSAL TUBING is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Med-Logics, Inc.. The 510(k) number is K983448.

When did ML UNIVERSAL TUBING receive FDA 510(k) clearance?

ML UNIVERSAL TUBING received FDA 510(k) clearance on 1998-12-18, under 510(k) number K983448.

Who is the listed applicant for ML UNIVERSAL 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 ML UNIVERSAL TUBING?

The FDA product code for ML UNIVERSAL TUBING is MSR.

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 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 ML7030K010353MED-LOGICS DISPOSABLE ALK TUBINGK002515MEDLOGICS ML 4000, MODEL 4000

View all 12 devices →

Related Devices (Code: MSR)

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.

K993361TUBING EXTENSION SETHurricane MedicalK980849SURGIN KITSurgin Surgical Instrumentation, Inc.K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKStorz Instrument Co.K972522ML-DISPOSABLE PAKMed-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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