FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Cross Wise™ Multi-Use RF Adapter Cable

K Number: K243193 · Decision Nov 26, 2024
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
19
Applicant Total
6
Review Days
57

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Basic Information

Device Name
Cross Wise™ Multi-Use RF Adapter Cable
K Number
K243193
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5175
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Circa Scientific, Inc.
Date Received
September 30, 2024
Decision Date
November 26, 2024
Product Code
DXF
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXF Catheter, Septostomy

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DXF), ordered by most recent decision date.

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Other Clearances by Circa Scientific, Inc.

K Number Device Name
K251007 CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C, CW-1085C, CW-1085V, CW-1013F)
K243954 PeriCross™ Epicardial Access Kit
K241414 CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C); CrossWise RF Adapter Cable (Model CW-1002)
K240004 CardioCurve Steerable Sheath Small Curl, 40cm (CC-1040S ); CardioCurve Steerable Sheath Medium Curl, 40cm (CC-1040M ); CardioCurve Steerable Sheath Large Curl, 40cm (CC-1040L ); CardioCurve Steerable Sheath Small Curl, 61cm (CC-1061S); CardioCurve Steerable Sheath Medium Curl, 61cm (CC-1061M ); CardioCurve Steerable Sheath Large Curl, 61cm (CC-1061L); CardioCurve Steerable Sheath Small Curl, 71cm (CC-1071S ); CardioCurve Steerable Sheath Medium Curl, 71cm (CC-1071M ); CardioCurve Steer
K222311 CIRCA MATRIX12 M Esophageal Temperature Probe and Temperature Monitoring System