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FDA 510(k)

GE LOGIQ A100 MP, MODEL 2272413

K-Number: K012560 · 2001-08-23

ApplicantGeneral Electric Co.
Decision Date2001-08-23
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

GE LOGIQ A100 MP, MODEL 2272413 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 2001-08-23 under 510(k) number K012560. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GE LOGIQ A100 MP, MODEL 2272413?

GE LOGIQ A100 MP, MODEL 2272413 is a medical device that received FDA 510(k) clearance on 2001-08-23. The listed applicant is General Electric Co.. The 510(k) number is K012560.

When did GE LOGIQ A100 MP, MODEL 2272413 receive FDA 510(k) clearance?

GE LOGIQ A100 MP, MODEL 2272413 received FDA 510(k) clearance on 2001-08-23, under 510(k) number K012560.

Who is the listed applicant for GE LOGIQ A100 MP, MODEL 2272413?

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 GE LOGIQ A100 MP, MODEL 2272413?

The FDA product code for GE LOGIQ A100 MP, MODEL 2272413 is IYO.

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Other records listing General Electric Co. as applicant

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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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