ClearanceBrief
Company ยท US

Amici, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 2007. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IYTSystem, Rebreathing, Radionuclide5
CAFNebulizer (Direct Patient Interface)3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 28, 2007K063716AEROSOL SYSTEM
Amici, Inc.
CAF
Mar 19, 1997K952910THE SWIRLER NEBULIZER
Amici, Inc.
CAF
Nov 3, 1995K952893THE SWIRLER AEROSOL SYSTEM
Amici, Inc.
CAF
Jan 14, 1991K904684AMICI KRYPTON ADMINISTRATION SYSTEM, MODIFICATION
Amici, Inc.
IYT
Jan 14, 1991K903805AMICI XENON ADMINISTRATION SET
Amici, Inc.
IYT
Oct 3, 1990K903694AMICI TRU-FIT SOFT PLASTIC MOUTHPIECE
Amici, Inc.
IYT
Feb 12, 1988K872920AMICI KRYPTON ADMINISTRATION SYSTEM*
Amici, Inc.
IYT
Mar 3, 1987K865084AMICI XENON REBREATHING SYSTEM*
Amici, Inc.
IYT

Latest recalls

DateFirm and productCodeLinked 510(k)
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