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FDA 510(k)

RT2600(115V)(220/240V) #H4008A & H4008AE

K-Number: K851807 · 1985-09-19

ApplicantGeneral Electric Co.
Decision Date1985-09-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RT2600(115V)(220/240V) #H4008A & H4008AE 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 1985-09-19 under 510(k) number K851807. 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 RT2600(115V)(220/240V) #H4008A & H4008AE?

RT2600(115V)(220/240V) #H4008A & H4008AE is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is General Electric Co.. The 510(k) number is K851807.

When did RT2600(115V)(220/240V) #H4008A & H4008AE receive FDA 510(k) clearance?

RT2600(115V)(220/240V) #H4008A & H4008AE received FDA 510(k) clearance on 1985-09-19, under 510(k) number K851807.

Who is the listed applicant for RT2600(115V)(220/240V) #H4008A & H4008AE?

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 RT2600(115V)(220/240V) #H4008A & H4008AE?

The FDA product code for RT2600(115V)(220/240V) #H4008A & H4008AE is IYO.

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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