Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AUTO-TENS MODEL VI DUAL CHANNEL BATT

K-Number: K833354 · 1983-11-28

Decision Date1983-11-28
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AUTO-TENS MODEL VI DUAL CHANNEL BATT is the device name listed in this FDA 510(k) record. The listed applicant is Physio Tronics Corp.. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833354. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

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.

↑