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FDA 510(k)

PARALYZED VETERANS OF AMERICA POWER RECLINER

K-Number: K883672 · 1988-09-13

ApplicantRolcontrol Products, Co., Inc.
Decision Date1988-09-13
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PARALYZED VETERANS OF AMERICA POWER RECLINER is the device name listed in this FDA 510(k) record. The listed applicant is Rolcontrol Products, Co., Inc.. It received FDA 510(k) clearance on 1988-09-13 under 510(k) number K883672. 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 PARALYZED VETERANS OF AMERICA POWER RECLINER?

PARALYZED VETERANS OF AMERICA POWER RECLINER is a medical device that received FDA 510(k) clearance on 1988-09-13. The listed applicant is Rolcontrol Products, Co., Inc.. The 510(k) number is K883672.

When did PARALYZED VETERANS OF AMERICA POWER RECLINER receive FDA 510(k) clearance?

PARALYZED VETERANS OF AMERICA POWER RECLINER received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883672.

Who is the listed applicant for PARALYZED VETERANS OF AMERICA POWER RECLINER?

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

What is the FDA product code for PARALYZED VETERANS OF AMERICA POWER RECLINER?

The FDA product code for PARALYZED VETERANS OF AMERICA POWER RECLINER is ITI.

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Other records listing Rolcontrol Products, Co., 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.

K885104LAYDOWN ARM SUPPORT MECHANISMK885106REMOVABLE BATTERY POWER SYSTEMK8851031600 LIGHT TOUCH CONTROLK885105SLIDING ARM SUPPORTK883673POWER MECHANICAL RECLINERK883679WHEELS-OFF QUICK RELEASE AXLE SYSTEM

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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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