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Qmed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Known Names

q-med, qmed

Recent 510(k) Clearances

K-NumberDeviceDate
K972991MONITOR ONE NDXDecember 3, 1998
K932109PROFILOMATDecember 3, 1993
K921476INTERP-1000October 21, 1992
K897121QEKG ELECTROCARDIOGRAPHApril 30, 1990
K873591A.R.M. (ASPEN RETURN MONITOR)September 30, 1987
K862377QMED SELF ADHERING ELECTRODESeptember 26, 1986
K863091BICORD BY QMEDAugust 29, 1986
K861437QMED SYSTEM 2150May 20, 1986
K843559KLEENIT BY QMEDOctober 24, 1984
K841172MONITOR ONEJuly 27, 1984
K840465Q-MED ELECTRODEJune 19, 1984