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FDA 510(k)

MEDAID DUAL CHANNEL TENS

K-Number: K834334 · 1984-02-13

ApplicantPar Medex , Ltd.
Decision Date1984-02-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MEDAID DUAL CHANNEL TENS is the device name listed in this FDA 510(k) record. The listed applicant is Par Medex , Ltd.. It received FDA 510(k) clearance on 1984-02-13 under 510(k) number K834334. 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 MEDAID DUAL CHANNEL TENS?

MEDAID DUAL CHANNEL TENS is a medical device that received FDA 510(k) clearance on 1984-02-13. The listed applicant is Par Medex , Ltd.. The 510(k) number is K834334.

When did MEDAID DUAL CHANNEL TENS receive FDA 510(k) clearance?

MEDAID DUAL CHANNEL TENS received FDA 510(k) clearance on 1984-02-13, under 510(k) number K834334.

Who is the listed applicant for MEDAID DUAL CHANNEL TENS?

The FDA 510(k) record lists Par Medex , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDAID DUAL CHANNEL TENS?

The FDA product code for MEDAID DUAL CHANNEL TENS is GZJ.

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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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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