HIVOX OTC Electrical Stimulator, FT610-B
K-Number: K211403 · 2021-10-15
Device Summary
Frequently Asked Questions
What is the HIVOX OTC Electrical Stimulator, FT610-B?
HIVOX OTC Electrical Stimulator, FT610-B is a medical device that received FDA 510(k) clearance on 2021-10-15. The listed applicant is Hivox Biotek, Inc.. The 510(k) number is K211403.
When did HIVOX OTC Electrical Stimulator, FT610-B receive FDA 510(k) clearance?
HIVOX OTC Electrical Stimulator, FT610-B received FDA 510(k) clearance on 2021-10-15, under 510(k) number K211403.
Who is the listed applicant for HIVOX OTC Electrical Stimulator, FT610-B?
The FDA 510(k) record lists Hivox Biotek, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HIVOX OTC Electrical Stimulator, FT610-B?
The FDA product code for HIVOX OTC Electrical Stimulator, FT610-B is NUH.
Other records listing Hivox Biotek, 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.