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FDA 510(k)

M.D.C. PORTA-LIFT

K-Number: K901793 · 1990-05-24

ApplicantMetal Dynamics Corp.
Decision Date1990-05-24
Product CodeING
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

M.D.C. PORTA-LIFT is the device name listed in this FDA 510(k) record. The listed applicant is Metal Dynamics Corp.. It received FDA 510(k) clearance on 1990-05-24 under 510(k) number K901793. The device is classified under product code ING. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the M.D.C. PORTA-LIFT?

M.D.C. PORTA-LIFT is a medical device that received FDA 510(k) clearance on 1990-05-24. The listed applicant is Metal Dynamics Corp.. The 510(k) number is K901793.

When did M.D.C. PORTA-LIFT receive FDA 510(k) clearance?

M.D.C. PORTA-LIFT received FDA 510(k) clearance on 1990-05-24, under 510(k) number K901793.

Who is the listed applicant for M.D.C. PORTA-LIFT?

The FDA 510(k) record lists Metal Dynamics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for M.D.C. PORTA-LIFT?

The FDA product code for M.D.C. PORTA-LIFT is ING.

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 Metal Dynamics Corp. 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.

K901794AIR CUSHIONED AUTO WHEELCHAIR LIFT ACL-200/AG-Z2

Related Devices (Code: ING)

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.

K113065RL, UL, SL, EL, AND EPL VERTICAL PLATFORM LIFTSBella Elevator, LLCK110495LIFTKAR PTSano Transportgerate GmbHK102088JOURNEY INCLINED PLATFORM LIFT AND SUPRA CURVED INCLINE PLATFORM LIFTThyssenkrupp Ceteco SrlK091881RPL/CPL VERTICAL PLATFORM LIFTSHarmar Summit, LLCK090856JOURNEY (OR RPSP), JOURNEY CUBIC (OR SUPRA OR TP02)Thyssenkrupp Ceteco SrlK073513MERITS E700 PORCE LIFTMerits Health Products Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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