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FDA 510(k)

E275

K-Number: K032653 · 2003-09-12

ApplicantMicro Current Technology, Inc.
Decision Date2003-09-12
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

E275 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 2003-09-12 under 510(k) number K032653. 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 E275?

E275 is a medical device that received FDA 510(k) clearance on 2003-09-12. The listed applicant is Micro Current Technology, Inc.. The 510(k) number is K032653.

When did E275 receive FDA 510(k) clearance?

E275 received FDA 510(k) clearance on 2003-09-12, under 510(k) number K032653.

Who is the listed applicant for E275?

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 E275?

The FDA product code for E275 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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