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FDA 510(k)

ML-DISPOSABLE PAK

K-Number: K972522 · 1997-09-30

ApplicantMed-Logics, Inc.
Decision Date1997-09-30
Product CodeMSR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ML-DISPOSABLE PAK 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 1997-09-30 under 510(k) number K972522. 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-DISPOSABLE PAK?

ML-DISPOSABLE PAK is a medical device that received FDA 510(k) clearance on 1997-09-30. The listed applicant is Med-Logics, Inc.. The 510(k) number is K972522.

When did ML-DISPOSABLE PAK receive FDA 510(k) clearance?

ML-DISPOSABLE PAK received FDA 510(k) clearance on 1997-09-30, under 510(k) number K972522.

Who is the listed applicant for ML-DISPOSABLE PAK?

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-DISPOSABLE PAK?

The FDA product code for ML-DISPOSABLE PAK is MSR.

Related Clinical Trials

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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

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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 MedicalK983448ML UNIVERSAL TUBINGMed-Logics, Inc.K980849SURGIN KITSurgin Surgical Instrumentation, Inc.K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKStorz Instrument Co.

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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