ClearanceBrief
Company ยท US

Adroit Medical Systems, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2008. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DWJSystem, Thermal Regulating2
ILOPack, Hot Or Cold, Water Circulating2
FMWCover, Mattress (Medical Purposes)1
KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 6, 2008K073712SOFT AIR, MODEL SA 4000 AND MISTRAL AIR, MODEL MA0100
Adroit Medical Systems, Inc.
DWJ
Jan 29, 1998K973981SAFEPASS STERILIZATION POUCH
Adroit Medical Systems, Inc.
KCT
Sep 10, 1997K970197HTP-1500 LOCALIZED HEAT THERAPY PUMP
Adroit Medical Systems, Inc.
ILO
Jan 10, 1997K962983STERILE SOFT-TEMP
Adroit Medical Systems, Inc.
ILO
Dec 11, 1992K921920SOFT-TEMP
Adroit Medical Systems, Inc.
DWJ
Nov 6, 1992K921928SOFT-COVER
Adroit Medical Systems, Inc.
FMW

Latest recalls

DateFirm and productCodeLinked 510(k)
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