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FDA 510(k)

DITER ULTRASONIC S 3000

K-Number: K901950 · 1990-07-27

ApplicantDiter Elektroniikka OY
Decision Date1990-07-27
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DITER ULTRASONIC S 3000 is the device name listed in this FDA 510(k) record. The listed applicant is Diter Elektroniikka OY. It received FDA 510(k) clearance on 1990-07-27 under 510(k) number K901950. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DITER ULTRASONIC S 3000?

DITER ULTRASONIC S 3000 is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Diter Elektroniikka OY. The 510(k) number is K901950.

When did DITER ULTRASONIC S 3000 receive FDA 510(k) clearance?

DITER ULTRASONIC S 3000 received FDA 510(k) clearance on 1990-07-27, under 510(k) number K901950.

Who is the listed applicant for DITER ULTRASONIC S 3000?

The FDA 510(k) record lists Diter Elektroniikka OY as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DITER ULTRASONIC S 3000?

The FDA product code for DITER ULTRASONIC S 3000 is IMI.

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Related Devices (Code: IMI)

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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.

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