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

EAGLE SYSTEM

K Number: K912799 · Decision Dec 18, 1991
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
120
Applicant Total
82
Review Days
176

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Basic Information

Device Name
EAGLE SYSTEM
K Number
K912799
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2040
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Marquette Electronics, Inc.
Date Received
June 25, 1991
Decision Date
December 18, 1991
Product Code
LMC
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
LMC Camera, Multi Format, Radiological

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Other Clearances by Marquette Electronics, Inc.

K Number Device Name
K971868 IMPACT (INFORMING MOBILE PERSONNEL AND CARE TRACKING) PAGER SYSTEM
K971683 WIRELESS LAN (LOCAL AREA NETWORK) - WIRELESS ETHERNET
K972199 SIGNAL-AVERAGED HIGH RESOLUTION P WAVE ANALYSIS
K962547 CARDIOSERV P
K963120 RESPONDER 2500 DEFIBRILLATOR AND CARDIAC CARE SYSTEM
K962827 ALARM DISPLAY UNIT/PAGER-LAN SYSTEM (ADU)
K964750 EAGLE 4000 PATIENT MONITOR
K962551 CARDIOSERV S
K960418 EAGLE PATIENT MONITOR
K960272 EAGLE 3000/3100 PATIENT MONITOR
Search all 82 clearances from Marquette Electronics, Inc. →