PORTALCAST— 510(k) K860193

Substantially Equivalent

Diacor, Inc.

FDA 510(k) clearance K860193 for PORTALCAST, Substantially Equivalent on 1986-01-30. Applicant: Diacor, Inc.. Device class: 2.

Clearance details

Applicant: Diacor, Inc.
Product code: Code IXI
Device class: Class 2
Regulation: 21 CFR 892.5710
Advisory panel: Radiology
Date received: 1986-01-22
Decision date: 1986-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code IXI

K253025 — Ricoh 3D for Healthcare Bolus2026-04-06
K222639 — VHA Radiotherapy Bolus2022-11-04
K214093 — VSP Bolus2022-03-30
K132236 — .DECIMAL PROTON APERTURE2013-10-16
K131150 — CURA COMPENSATOR2013-07-30

More clearances from Diacor, Inc.

K121929 — ZEPHYR 'X-SERIES PATIENT TRANSFER SLED2013-01-17
K050888 — INTEGRA IMMOBILIZATION SYSTEM2005-05-23
K954414 — CENTRALITE BACKPOINTER1995-10-23
K953046 — PERI-PUSHER1995-09-22
K950112 — CENTRALITE(R)-DLL SERIES1995-08-16

Data sourced from openFDA. This site is unofficial and independent of the FDA.