ALEVE Direct Therapy (ALEVE Direct Therapy TENS device)

FDA 510(k) K152852 · Bayer Healthcare, LLC

Substantially Equivalent

510(k) numberK152852

Submission

Device name
ALEVE Direct Therapy (ALEVE Direct Therapy TENS device)
Applicant
Bayer Healthcare, LLC
Whippany, NJ, US
Received
September 29, 2015
Decision date
December 22, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NUH – Stimulator, Nerve, Transcutaneous, Over-The-Counter
Device class
Class II (moderate risk)
Regulation
21 CFR 882.5890
Specialty
Neurology

TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES

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Questions and answers

When was ALEVE Direct Therapy (ALEVE Direct Therapy TENS device) cleared by the FDA?

ALEVE Direct Therapy (ALEVE Direct Therapy TENS device) (K152852) received a 510(k) decision of Substantially Equivalent on December 22, 2015, 84 days after the submission was received.

What is the product code of K152852?

The FDA product code is NUH – Stimulator, Nerve, Transcutaneous, Over-The-Counter, a Class II (moderate risk) device regulated under 21 CFR 882.5890.