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FDA 510(k)

MICRO-PROCESSOR UNIT #A3600AC

K-Number: K801762 · 1980-08-27

ApplicantGeneral Electric Co.
Decision Date1980-08-27
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICRO-PROCESSOR UNIT #A3600AC 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 1980-08-27 under 510(k) number K801762. 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-PROCESSOR UNIT #A3600AC?

MICRO-PROCESSOR UNIT #A3600AC is a medical device that received FDA 510(k) clearance on 1980-08-27. The listed applicant is General Electric Co.. The 510(k) number is K801762.

When did MICRO-PROCESSOR UNIT #A3600AC receive FDA 510(k) clearance?

MICRO-PROCESSOR UNIT #A3600AC received FDA 510(k) clearance on 1980-08-27, under 510(k) number K801762.

Who is the listed applicant for MICRO-PROCESSOR UNIT #A3600AC?

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-PROCESSOR UNIT #A3600AC?

The FDA product code for MICRO-PROCESSOR UNIT #A3600AC 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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