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FDA 510(k)

NOVA TRANSFER SYSTEM, MODEL XXX

K-Number: K874448 · 1987-12-17

ApplicantNova Technology Corp.
Decision Date1987-12-17
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NOVA TRANSFER SYSTEM, MODEL XXX is the device name listed in this FDA 510(k) record. The listed applicant is Nova Technology Corp.. It received FDA 510(k) clearance on 1987-12-17 under 510(k) number K874448. 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 NOVA TRANSFER SYSTEM, MODEL XXX?

NOVA TRANSFER SYSTEM, MODEL XXX is a medical device that received FDA 510(k) clearance on 1987-12-17. The listed applicant is Nova Technology Corp.. The 510(k) number is K874448.

When did NOVA TRANSFER SYSTEM, MODEL XXX receive FDA 510(k) clearance?

NOVA TRANSFER SYSTEM, MODEL XXX received FDA 510(k) clearance on 1987-12-17, under 510(k) number K874448.

Who is the listed applicant for NOVA TRANSFER SYSTEM, MODEL XXX?

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

What is the FDA product code for NOVA TRANSFER SYSTEM, MODEL XXX?

The FDA product code for NOVA TRANSFER SYSTEM, MODEL XXX 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 Nova Technology 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.

K963701SOMA SAFE ENCLOSUREK964246NOVABED PATIENT TRANSFER 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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