ClearanceBrief
Company ยท US

Cathlab Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1991. 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
DXECatheter, Embolectomy4
DQOCatheter, Intravascular, Diagnostic1
DQTOccluder, Catheter Tip1
DYGCatheter, Flow Directed1
GCABiliary Catheter For Stone Removal That May Also Allow For Irrigation And Contrast Injection1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 2, 1991K910917CATHLAB SILICONE BILIARY BALLOON CATHETER
Cathlab Corp.
GCA
Jun 24, 1991K910916CATHLAB SILICONE OCCLUSION BALLOON CATHETER
Cathlab Corp.
DQT
Feb 25, 1991K905139CATHLAB SILICONE ARTERIAL EMBOLECTOMY CATHETER
Cathlab Corp.
DXE
Mar 16, 1990K897051MILLER PERCUTANEOUS ANGIOGRAPHIC/SCOPIC IRRI. CATH
Cathlab Corp.
DQO
Mar 14, 1990K8971843F AND 4F IRRIGATION EMBOLECTOMY CATHETERS
Cathlab Corp.
DXE
Sep 26, 1989K893435SILICONE FLOW-DIRECTED THERMODILUTION CATHETER
Cathlab Corp.
DYG
Aug 1, 1989K893680SILICONE BI-LUMEN IRRIGATION EMBOLECTOMY CATH.
Cathlab Corp.
DXE
Jun 15, 1988K881455EMBOLECTOMY CATHETER(MODIFIED)
Cathlab Corp.
DXE

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes