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FDA 510(k)

MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.

K-Number: K881461 · 1988-07-18

ApplicantDufco Electronics, Inc.
Decision Date1988-07-18
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. is the device name listed in this FDA 510(k) record. The listed applicant is Dufco Electronics, Inc.. It received FDA 510(k) clearance on 1988-07-18 under 510(k) number K881461. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.?

MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Dufco Electronics, Inc.. The 510(k) number is K881461.

When did MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. receive FDA 510(k) clearance?

MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. received FDA 510(k) clearance on 1988-07-18, under 510(k) number K881461.

Who is the listed applicant for MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.?

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

What is the FDA product code for MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH.?

The FDA product code for MULTIMODE(TM) INTERFACE SYSTEM FOR MEYRA WHEELCH. is ITI.

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 Dufco Electronics, 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.

K881464MULTIMODE(TM) INTERFACE SYS. FOR EVEREST & JENNINGK881463MULTIMODE(TM) POWER MODULE SYSTEMK881462UNIMODE(TM) POWER MODULE SYSTEM

Related Devices (Code: ITI)

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.

K262582Electric wheelchair (GP100)Suzhou Green Pine Medical Co., Ltd.K262054Electric WheelchairYongkang Joymax Medical Technology Co., Ltd.K260053Power Wheelchair (OS-R-M01I)Beijing OrionStar Technology Co., Ltd.K260229Electric wheelchair (HC819N, HC830N, HC831N)Yongkang Hengyi Vehicle Co., Ltd.K261354Electric wheelchair (D03)Foshan Sowell Medical Technology Co., Ltd.K261149Electric Wheelchair (DY611A-2, DY612A-1)Zhejiang Lumbre Electric Appliance 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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