PATIENT DOSE MONITOR— 510(k) K912249

Substantially Equivalent

Theta Systems, Inc.

FDA 510(k) clearance K912249 for PATIENT DOSE MONITOR, Substantially Equivalent on 1991-08-30. Applicant: Theta Systems, Inc.. Device class: 2.

Clearance details

Applicant: Theta Systems, Inc.
Product code: Code KPZ
Device class: Class 2
Regulation: 21 CFR 892.5900
Advisory panel: Radiology
Date received: 1991-05-21
Decision date: 1991-08-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melbourne, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPZ

K860469 — 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS1986-04-16
K854410 — VERIFLEX1986-02-12

More clearances from Theta Systems, Inc.

K912250 — ISORAD(TM) INTEGRAL BUILDUP PHOTON DIODES1991-11-05

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