Home Care Vareious Models of Powered Muscle Stimulator, HT-311, HT-311N, HT-312

FDA 510(k) K022998 · Home Care Technology Co., Ltd.

Substantially Equivalent

510(k) numberK022998

Submission

Device name
Home Care Vareious Models of Powered Muscle Stimulator, HT-311, HT-311N, HT-312
Applicant
Home Care Technology Co., Ltd.
Columbus, OH, US
Received
September 9, 2002
Decision date
May 20, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
IPF – Stimulator, Muscle, Powered
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5850
Specialty
Physical Medicine

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More from Sunmed, LLC

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Questions and answers

When was Home Care Vareious Models of Powered Muscle Stimulator, HT-311, HT-311N, HT-312 cleared by the FDA?

Home Care Vareious Models of Powered Muscle Stimulator, HT-311, HT-311N, HT-312 (K022998) received a 510(k) decision of Substantially Equivalent on May 20, 2003, 253 days after the submission was received.

What is the product code of K022998?

The FDA product code is IPF – Stimulator, Muscle, Powered, a Class II (moderate risk) device regulated under 21 CFR 890.5850.