ClearanceBrief
Company ยท US

Crossbay Medical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2014 to 2020. 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
HHKCurette, Suction, Endometrial (And Accessories)2
LKFCannula, Manipulator/Injector, Uterine1
MQFCatheter, Assisted Reproduction1
PGKCannula, Injector, Uterine, Endometrial Biopsy1
PONCatheter, Balloon, Dilation Of Cervical Canal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 5, 2020K201952CrossGlide ETS Plus
Crossbay Medical
HHK
Mar 25, 2020K192534CrossBay Endometrial Tissue Sampler (ETS)
Crossbay Medical
HHK
Aug 23, 2019K190813CrossBay Cervical Dilator Catheter System
Crossbay Medical
PON
Jan 5, 2017K162064CrossBay IVF Embryo Transfer Catheter Set
Crossbay Medical, Inc.
MQF
Mar 20, 2015K142545SonoFlow Sonohysterography and Sonohysterosalpingography Device
Crossbay Medical, Inc.
LKF
Mar 19, 2014K133144SONOSURE SONOHYSTEROGRAPHY & ENDOMETRIAL SAMPLING DEVICE
Crossbay Medical, Inc.
PGK

Latest recalls

DateFirm and productCodeLinked 510(k)
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