FDA 510(k) FDA class 1 Substantially Equivalent 🇸🇪 Sweden

DIOLASE

K Number: K904753 · Decision Nov 9, 1990
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
27
Applicant Total
7
Review Days
21

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Basic Information

Device Name
DIOLASE
K Number
K904753
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.5780
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Scanditronix, Inc.
Date Received
October 19, 1990
Decision Date
November 9, 1990
Product Code
IWE
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
IWE Monitor, Patient Position, Light-Beam

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K Number Device Name
K934303 RFA A-300
K942092 DPD-3
K925133 DPD-510 THERAPEUTIC RADIATION DOSIMETER
K914926 SCANDIPLAN - VERSION 338
K900434 MM-22 MICROTRON, MM50 MICROTRON
K843366 SUPERPETT