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FDA 510(k)

P&F POWER WHEELCHAIR, HC-510

K-Number: K070350 · 2007-03-14

ApplicantP & F Brother Ind., Corp.
Decision Date2007-03-14
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

P&F POWER WHEELCHAIR, HC-510 is the device name listed in this FDA 510(k) record. The listed applicant is P & F Brother Ind., Corp.. It received FDA 510(k) clearance on 2007-03-14 under 510(k) number K070350. 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 P&F POWER WHEELCHAIR, HC-510?

P&F POWER WHEELCHAIR, HC-510 is a medical device that received FDA 510(k) clearance on 2007-03-14. The listed applicant is P & F Brother Ind., Corp.. The 510(k) number is K070350.

When did P&F POWER WHEELCHAIR, HC-510 receive FDA 510(k) clearance?

P&F POWER WHEELCHAIR, HC-510 received FDA 510(k) clearance on 2007-03-14, under 510(k) number K070350.

Who is the listed applicant for P&F POWER WHEELCHAIR, HC-510?

The FDA 510(k) record lists P & F Brother Ind., Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for P&F POWER WHEELCHAIR, HC-510?

The FDA product code for P&F POWER WHEELCHAIR, HC-510 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 P & F Brother Ind., 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.

K082722P & F POWER WHEELCHAIR, MODEL HC-500SB

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

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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