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FDA 510(k)

PERMOBIL MAXIOR

K-Number: K870224 · 1987-02-10

ApplicantPermobil of America
Decision Date1987-02-10
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PERMOBIL MAXIOR is the device name listed in this FDA 510(k) record. The listed applicant is Permobil of America. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K870224. 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 PERMOBIL MAXIOR?

PERMOBIL MAXIOR is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Permobil of America. The 510(k) number is K870224.

When did PERMOBIL MAXIOR receive FDA 510(k) clearance?

PERMOBIL MAXIOR received FDA 510(k) clearance on 1987-02-10, under 510(k) number K870224.

Who is the listed applicant for PERMOBIL MAXIOR?

The FDA 510(k) record lists Permobil of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERMOBIL MAXIOR?

The FDA product code for PERMOBIL MAXIOR 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 Permobil of America 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.

K870226PERMOBIL MINIORK870228PERMOBIL HEXIORK870227PERMOBIL SUPERIORK870225PERMOBIL EXTERIOR

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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