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FDA 510(k)

TK40 - TILTMASTER

K-Number: K961744 · 1996-07-25

ApplicantMechanical Application Designs, Inc.
Decision Date1996-07-25
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TK40 - TILTMASTER 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 1996-07-25 under 510(k) number K961744. 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 TK40 - TILTMASTER?

TK40 - TILTMASTER is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Mechanical Application Designs, Inc.. The 510(k) number is K961744.

When did TK40 - TILTMASTER receive FDA 510(k) clearance?

TK40 - TILTMASTER received FDA 510(k) clearance on 1996-07-25, under 510(k) number K961744.

Who is the listed applicant for TK40 - TILTMASTER?

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 TK40 - TILTMASTER?

The FDA product code for TK40 - TILTMASTER 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.

K972564TILT MASTER CG SYSTEM (CENTER OF GRAVITY), TILT-N-SPACE-SEATK972563LIFT MASTER

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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