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FDA 510(k)

TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT

K-Number: K972564 · 1997-08-25

ApplicantMechanical Application Designs, Inc.
Decision Date1997-08-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT is the device name listed in this FDA 510(k) record. The listed applicant is Mechanical Application Designs, Inc.. It received FDA 510(k) clearance on 1997-08-25 under 510(k) number K972564. 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 TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT?

TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT is a medical device that received FDA 510(k) clearance on 1997-08-25. The listed applicant is Mechanical Application Designs, Inc.. The 510(k) number is K972564.

When did TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT receive FDA 510(k) clearance?

TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT received FDA 510(k) clearance on 1997-08-25, under 510(k) number K972564.

Who is the listed applicant for TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT?

The FDA 510(k) record lists Mechanical Application Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT?

The FDA product code for TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEAT 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 Mechanical Application Designs, 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.

K972563LIFT MASTERK961744TK40 - TILTMASTER

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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