ClearanceBrief
Company ยท US

Dornoch Medical Systems, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2019. 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
JCXApparatus, Suction, Ward Use, Portable, Ac-Powered6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 24, 2019K190789IntelliCartTM System
Dornoch Medical Systems
JCX
Sep 14, 2017K172481IntelliCart System
Dornoch Medical Systems
JCX
Dec 21, 2016K162421IntelliCartTM System
Dornoch Medical Systems
JCX
Mar 21, 2014K133786DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID
Dornoch Medical Systems, Inc.
JCX
Mar 4, 2013K123188DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MODEL UL-DU500, DORNOC
Dornoch Medical Systems, Inc.
JCX
Apr 29, 2008K081047TRANSPOSAL ULTRA SYSTEMS
Dornoch Medical Systems, Inc.
JCX

Latest recalls

DateFirm and productCodeLinked 510(k)
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