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FDA 510(k)

AXON II BRAND OF DUAL CHANNEL TENS

K-Number: K850860 · 1985-05-31

ApplicantCassandra Electronics Corp.
Decision Date1985-05-31
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

AXON II BRAND OF DUAL CHANNEL TENS is the device name listed in this FDA 510(k) record. The listed applicant is Cassandra Electronics Corp.. It received FDA 510(k) clearance on 1985-05-31 under 510(k) number K850860. 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 AXON II BRAND OF DUAL CHANNEL TENS?

AXON II BRAND OF DUAL CHANNEL TENS is a medical device that received FDA 510(k) clearance on 1985-05-31. The listed applicant is Cassandra Electronics Corp.. The 510(k) number is K850860.

When did AXON II BRAND OF DUAL CHANNEL TENS receive FDA 510(k) clearance?

AXON II BRAND OF DUAL CHANNEL TENS received FDA 510(k) clearance on 1985-05-31, under 510(k) number K850860.

Who is the listed applicant for AXON II BRAND OF DUAL CHANNEL TENS?

The FDA 510(k) record lists Cassandra Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AXON II BRAND OF DUAL CHANNEL TENS?

The FDA product code for AXON II BRAND OF 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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