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

MONITOR ONE NDX

K Number: K972991 · Decision Dec 3, 1998
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
11
Review Days
478

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Basic Information

Device Name
MONITOR ONE NDX
K Number
K972991
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Qmed, Inc.
Date Received
August 12, 1997
Decision Date
December 3, 1998
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Qmed, Inc.

K Number Device Name
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
K841172 MONITOR ONE
K840465 Q-MED ELECTRODE
Search all 11 clearances from Qmed, Inc. →