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FDA 510(k)

MED-4000

K-Number: K993823 · 1999-11-19

ApplicantMicro Current Technology, Inc.
Decision Date1999-11-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MED-4000 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Current Technology, Inc.. It received FDA 510(k) clearance on 1999-11-19 under 510(k) number K993823. 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 MED-4000?

MED-4000 is a medical device that received FDA 510(k) clearance on 1999-11-19. The listed applicant is Micro Current Technology, Inc.. The 510(k) number is K993823.

When did MED-4000 receive FDA 510(k) clearance?

MED-4000 received FDA 510(k) clearance on 1999-11-19, under 510(k) number K993823.

Who is the listed applicant for MED-4000?

The FDA 510(k) record lists Micro Current Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MED-4000?

The FDA product code for MED-4000 is GZJ.

Other records listing Micro Current Technology, Inc. as applicant

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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

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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