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

MONITOR ONE

K Number: K841172 · Decision Jul 27, 1984
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
11
Review Days
130

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Basic Information

Device Name
MONITOR ONE
K Number
K841172
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Qmed, Inc.
Date Received
March 19, 1984
Decision Date
July 27, 1984
Product Code
DSI
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DSI Detector And Alarm, Arrhythmia

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Other Clearances by Qmed, Inc.

K Number Device Name
K972991 MONITOR ONE NDX
K932109 PROFILOMAT
K921476 INTERP-1000
K897121 QEKG ELECTROCARDIOGRAPH
K873591 A.R.M. (ASPEN RETURN MONITOR)
K862377 QMED SELF ADHERING ELECTRODE
K863091 BICORD BY QMED
K861437 QMED SYSTEM 2150
K843559 KLEENIT BY QMED
K840465 Q-MED ELECTRODE
Search all 11 clearances from Qmed, Inc. →