FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MLC FIT

K Number: K991133 · Decision Mar 27, 2000
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
13
Review Days
360

Basic Information

Device Name
MLC FIT
K Number
K991133
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
IMPAC MEDICAL SYSTEMS, INC.
Date Received
April 2, 1999
Decision Date
March 27, 2000
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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Other Clearances by IMPAC MEDICAL SYSTEMS, INC.

K Number Device Name
K151233 Monaco
K141572 MOSAIQ ONCOLOGY INFORMATION SYSTEM
K132971 MONACO
K123230 MOSAIQ ONCOLOGY INFORMATION SYSTEM
K120067 MOSAIQ ONCOLOGY INFORMATION SYSTEM
K043412 MODIFICATION TO: VIEWSTATION
K013531 QWIKSIM VIRTUAL SIMULATION SYSTEM; VERSION 2.00
K011694 VIEWSTATION
K981313 SEQUENCER
K962335 MLC FIT
Search all 13 clearances from IMPAC MEDICAL SYSTEMS, INC. →