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Reimers Systems, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K102831
RSI 4200
August 19, 2011
K962871
ODS1 - HOOD DRIVER
October 23, 1996
K962869
GSP1 - GAS SELECTION PANEL
October 23, 1996
K954387
T CLASS HYPERBARIC FACILITIES
December 15, 1995
K951125
LIFEFORCE CLINICAL HYPERBARIC FACILITY
June 2, 1995