ClearanceBrief
Company ยท US

Dms Products, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1989. 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
JSSKit, Identification, Enterobacteriaceae2
JSTKit, Fastidious Organisms1
JTODiscs, Strips And Reagents, Microorganism Differentiation1
JXAKit, Screening, Urine1
LQLGram Positive Identification Panel1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 9, 1989K891004RAPIDEC STAPH
Dms Products, Inc.
LQL
Sep 26, 1989K894805RAPIDEC UR
Dms Products, Inc.
JXA
Jun 2, 1989K890626RAPIDEC COLI
Dms Products, Inc.
JSS
Feb 17, 1989K890625JAMES REAGENT
Dms Products, Inc.
JTO
Mar 6, 1986K854733API 20 EC (ENTEROBACTERIACEAE)(IDENTIFICATION KIT)
Dms Products, Inc.
JSS
Mar 4, 1986K854732API 50 CHB (CULTURE MEDIA)
Dms Products, Inc.
JST

Latest recalls

DateFirm and productCodeLinked 510(k)
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