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FDA 510(k)

ESI MODEL MS-103

K-Number: K885120 · 1990-01-19

ApplicantElectrical Systems Div.
Decision Date1990-01-19
Product CodeGZT
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ESI MODEL MS-103 is the device name listed in this FDA 510(k) record. The listed applicant is Electrical Systems Div.. It received FDA 510(k) clearance on 1990-01-19 under 510(k) number K885120. The device is classified under product code GZT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ESI MODEL MS-103?

ESI MODEL MS-103 is a medical device that received FDA 510(k) clearance on 1990-01-19. The listed applicant is Electrical Systems Div.. The 510(k) number is K885120.

When did ESI MODEL MS-103 receive FDA 510(k) clearance?

ESI MODEL MS-103 received FDA 510(k) clearance on 1990-01-19, under 510(k) number K885120.

Who is the listed applicant for ESI MODEL MS-103?

The FDA 510(k) record lists Electrical Systems Div. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESI MODEL MS-103?

The FDA product code for ESI MODEL MS-103 is GZT.

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Official Source

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