FDA 510(k)

MEA110

K-Number: K843822 · 1984-10-22

Decision Date1984-10-22

Product CodeGZJ

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MEA110 is the device name listed in this FDA 510(k) record. The listed applicant is Canadian Medical Products. It received FDA 510(k) clearance on 1984-10-22 under 510(k) number K843822. 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 MEA110?

MEA110 is a medical device that received FDA 510(k) clearance on 1984-10-22. The listed applicant is Canadian Medical Products. The 510(k) number is K843822.

When did MEA110 receive FDA 510(k) clearance?

MEA110 received FDA 510(k) clearance on 1984-10-22, under 510(k) number K843822.

Who is the listed applicant for MEA110?

The FDA 510(k) record lists Canadian Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEA110?

The FDA product code for MEA110 is GZJ.

Other records listing Canadian Medical Products 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.

K820326BIGSTON TRANSCUTANEOUS NERVE STIMULAT

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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.