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FDA 510(k)

RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE

K-Number: K863700 · 1987-02-10

ApplicantGeneral Electric Co.
Decision Date1987-02-10
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE 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 1987-02-10 under 510(k) number K863700. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE?

RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is General Electric Co.. The 510(k) number is K863700.

When did RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE receive FDA 510(k) clearance?

RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE received FDA 510(k) clearance on 1987-02-10, under 510(k) number K863700.

Who is the listed applicant for RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE?

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 RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE?

The FDA product code for RT2800(115V)/H4008C AND RT2800(220/240V)/H4008CE is ITX.

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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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