FDA 510(k)

EMG-UT 30

K-Number: K802390 · 1981-01-09

Decision Date1981-01-09

Product CodeHCC

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

EMG-UT 30 is the device name listed in this FDA 510(k) record. The listed applicant is American Scientific Corp.. It received FDA 510(k) clearance on 1981-01-09 under 510(k) number K802390. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMG-UT 30?

EMG-UT 30 is a medical device that received FDA 510(k) clearance on 1981-01-09. The listed applicant is American Scientific Corp.. The 510(k) number is K802390.

When did EMG-UT 30 receive FDA 510(k) clearance?

EMG-UT 30 received FDA 510(k) clearance on 1981-01-09, under 510(k) number K802390.

Who is the listed applicant for EMG-UT 30?

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

What is the FDA product code for EMG-UT 30?

The FDA product code for EMG-UT 30 is HCC.

Other records listing American Scientific Corp. 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.

K802391EMG-UT 40

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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.