BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1
K-Number: K062641 · 2007-04-30
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Device Summary
Frequently Asked Questions
What is the BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1?
BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1 is a medical device that received FDA 510(k) clearance on 2007-04-30. The listed applicant is Avazzia, Inc.. The 510(k) number is K062641.
When did BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1 receive FDA 510(k) clearance?
BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1 received FDA 510(k) clearance on 2007-04-30, under 510(k) number K062641.
Who is the listed applicant for BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1?
The FDA 510(k) record lists Avazzia, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1?
The FDA product code for BODY-STIM, BIOMODULATOR, BEST-RSI, BEST PRO, MODEL BEST-AV1 is GZJ.
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.
Other records listing Avazzia, 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: GZJ)
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.
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