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FDA 510(k)

MYVACET 5-07, 7-00 AND 9-40

K-Number: K791178 · 1979-09-17

ApplicantRadiation Products Design, Inc.
Decision Date1979-09-17
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MYVACET 5-07, 7-00 AND 9-40 is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Products Design, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791178. The device is classified under product code IXI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYVACET 5-07, 7-00 AND 9-40?

MYVACET 5-07, 7-00 AND 9-40 is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Radiation Products Design, Inc.. The 510(k) number is K791178.

When did MYVACET 5-07, 7-00 AND 9-40 receive FDA 510(k) clearance?

MYVACET 5-07, 7-00 AND 9-40 received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791178.

Who is the listed applicant for MYVACET 5-07, 7-00 AND 9-40?

The FDA 510(k) record lists Radiation Products Design, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYVACET 5-07, 7-00 AND 9-40?

The FDA product code for MYVACET 5-07, 7-00 AND 9-40 is IXI.

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Other records listing Radiation Products Design, Inc. as applicant

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Related Devices (Code: IXI)

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K253025Ricoh 3D for Healthcare BolusRicoh 3D For Healthcare, LLCK222639VHA Radiotherapy BolusVha DeanK214093VSP Bolus3D SystemsK132236.DECIMAL PROTON APERTURE.Decimal, Inc.K131150CURA COMPENSATORCura Medical Technologies, LLCK123893CURA COLLIMATORCura Medical Technologies, LLC

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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