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FDA 510(k)

MICRO-PREPROCESSOR UNIT

K-Number: K812914 · 1981-12-29

ApplicantGeneral Electric Co.
Decision Date1981-12-29
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO-PREPROCESSOR UNIT is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1981-12-29 under 510(k) number K812914. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO-PREPROCESSOR UNIT?

MICRO-PREPROCESSOR UNIT is a medical device that received FDA 510(k) clearance on 1981-12-29. The listed applicant is General Electric Co.. The 510(k) number is K812914.

When did MICRO-PREPROCESSOR UNIT receive FDA 510(k) clearance?

MICRO-PREPROCESSOR UNIT received FDA 510(k) clearance on 1981-12-29, under 510(k) number K812914.

Who is the listed applicant for MICRO-PREPROCESSOR UNIT?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-PREPROCESSOR UNIT?

The FDA product code for MICRO-PREPROCESSOR UNIT is DSI.

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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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