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

14 COLOR VIDEO DISPLAY 211-260-010

K Number: K893585 · Decision Jul 20, 1989
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
34
Review Days
72

Basic Information

Device Name
14 COLOR VIDEO DISPLAY 211-260-010
K Number
K893585
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
MENNEN MEDICAL, INC.
Date Received
May 9, 1989
Decision Date
July 20, 1989
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

View all

Other Clearances by MENNEN MEDICAL, INC.

K Number Device Name
K030722 ENVOY PATIENT MONITOR
K983864 ETCO2 VITAL SIGNS MODULE
K991775 MODIFICATION TO COMPUTERIZED CATHETERIZATION LABORATORY - HORIZON 9000 WS
K982697 MODIFICATION TO ENSEMBLE CENTRAL STATION MONITOR
K974510 ENVOY PATIENT MONITOR
K970358 ENSEMBLE CENTRAL STATION MONITOR
K940081 MERCURY
K940415 HORIZON 9000 WS
K920915 CAPNOMED 100 STAND-ALONE ETCO2 MODULE
K914381 HORIZON 9000/HIS OPTION AMPLIFIER
Search all 34 clearances from MENNEN MEDICAL, INC. →