Heat Pain Pro
K-Number: K181992 · 2018-11-09
Device Summary
Frequently Asked Questions
What is the Heat Pain Pro?
Heat Pain Pro is a medical device that received FDA 510(k) clearance on 2018-11-09. The listed applicant is Omron Healthcare, Inc.. The 510(k) number is K181992.
When did Heat Pain Pro receive FDA 510(k) clearance?
Heat Pain Pro received FDA 510(k) clearance on 2018-11-09, under 510(k) number K181992.
Who is the listed applicant for Heat Pain Pro?
The FDA 510(k) record lists Omron Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Heat Pain Pro?
The FDA product code for Heat Pain Pro is NUH.
Other records listing Omron Healthcare, 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.
Related Devices (Code: NUH)
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.
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.