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FDA 510(k)

PORTALCAST

K-Number: K860193 · 1986-01-30

ApplicantDiacor, Inc.
Decision Date1986-01-30
Product CodeIXI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PORTALCAST is the device name listed in this FDA 510(k) record. The listed applicant is Diacor, Inc.. It received FDA 510(k) clearance on 1986-01-30 under 510(k) number K860193. 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 PORTALCAST?

PORTALCAST is a medical device that received FDA 510(k) clearance on 1986-01-30. The listed applicant is Diacor, Inc.. The 510(k) number is K860193.

When did PORTALCAST receive FDA 510(k) clearance?

PORTALCAST received FDA 510(k) clearance on 1986-01-30, under 510(k) number K860193.

Who is the listed applicant for PORTALCAST?

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

What is the FDA product code for PORTALCAST?

The FDA product code for PORTALCAST is IXI.

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Other records listing Diacor, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K121929ZEPHYR 'X-SERIES PATIENT TRANSFER SLEDK050888INTEGRA IMMOBILIZATION SYSTEMK954414CENTRALITE BACKPOINTERK953046PERI-PUSHERK950112CENTRALITE(R)-DLL SERIESK934566RADASSIST

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Related Devices (Code: IXI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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