Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ML DISPOSABLE ALK TUBING

K-Number: K971173 · 1997-05-22

ApplicantMed-Logics, Inc.
Decision Date1997-05-22
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ML 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 1997-05-22 under 510(k) number K971173. 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 ML DISPOSABLE ALK TUBING?

ML DISPOSABLE ALK TUBING is a medical device that received FDA 510(k) clearance on 1997-05-22. The listed applicant is Med-Logics, Inc.. The 510(k) number is K971173.

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

ML DISPOSABLE ALK TUBING received FDA 510(k) clearance on 1997-05-22, under 510(k) number K971173.

Who is the listed applicant for ML 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 ML DISPOSABLE ALK TUBING?

The FDA product code for ML DISPOSABLE ALK TUBING is KYG.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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: 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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.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.

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.

↑