AUTO-TENS MODEL VI DUAL CHANNEL BATT
K-Number: K833354 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the AUTO-TENS MODEL VI DUAL CHANNEL BATT?
AUTO-TENS MODEL VI DUAL CHANNEL BATT is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Physio Tronics Corp.. The 510(k) number is K833354.
When did AUTO-TENS MODEL VI DUAL CHANNEL BATT receive FDA 510(k) clearance?
AUTO-TENS MODEL VI DUAL CHANNEL BATT received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833354.
Who is the listed applicant for AUTO-TENS MODEL VI DUAL CHANNEL BATT?
The FDA 510(k) record lists Physio Tronics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTO-TENS MODEL VI DUAL CHANNEL BATT?
The FDA product code for AUTO-TENS MODEL VI DUAL CHANNEL BATT 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.
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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