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FDA 510(k)

POWER MECHANICAL RECLINER

K-Number: K883673 · 1988-09-13

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

Device Summary

POWER MECHANICAL 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 K883673. 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 POWER MECHANICAL RECLINER?

POWER MECHANICAL 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 K883673.

When did POWER MECHANICAL RECLINER receive FDA 510(k) clearance?

POWER MECHANICAL RECLINER received FDA 510(k) clearance on 1988-09-13, under 510(k) number K883673.

Who is the listed applicant for POWER MECHANICAL 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 POWER MECHANICAL RECLINER?

The FDA product code for POWER MECHANICAL 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 SUPPORTK883679WHEELS-OFF QUICK RELEASE AXLE SYSTEMK883672PARALYZED VETERANS OF AMERICA POWER RECLINER

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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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