37-701-1 PATIENT DOASE MONITOR WITH DETECTORS— 510(k) K860469

Name: FDA 510(k) clearance K860469
Creator: U.S. Food and Drug Administration
Published: 1986-04-16

Substantially Equivalent

Victoreen, Inc.

FDA 510(k) clearance K860469 for 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS, Substantially Equivalent on 1986-04-16. Applicant: Victoreen, Inc.. Device class: 2.

Clearance details

Applicant: Victoreen, Inc.
Product code: Code KPZ
Device class: Class 2
Regulation: 21 CFR 892.5900
Advisory panel: Radiology
Date received: 1986-02-06
Decision date: 1986-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carle Place, NY, US

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K912249 — PATIENT DOSE MONITOR1991-08-30
K854410 — VERIFLEX1986-02-12

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K973960 — MODEL 37-1851998-01-14
K964952 — VERIDOSE V (FIVE), MODEL NUMBER 37-7051997-07-21
K964785 — VERIDOSE DIODES1997-06-13

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