FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇬 Singapore

Bioptimal Bipolar Pacing Catheter

K Number: K242863 · Decision Jun 15, 2025
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
128
Applicant Total
2
Review Days
268

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Basic Information

Device Name
Bioptimal Bipolar Pacing Catheter
K Number
K242863
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioptimal International Pte. , Ltd.
Date Received
September 20, 2024
Decision Date
June 15, 2025
Product Code
LDF
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
LDF Electrode, Pacemaker, Temporary

Similar 510(k) Clearances

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

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Other Clearances by Bioptimal International Pte. , Ltd.

K Number Device Name
K252702 Bioptimal Pulmonary Artery Monitoring Catheter (TD2502NF, TD2502NGF, TD2502NDF, TD2502NCF, TD2502NCGF, TD2502NDGF, TD2502NDCF, TD2502NDCGF, TD2502NXCF, TD2502NDXF, TD2502NXCGF, TD2502NDXGF, TD2502NDXCF, TD2502NDXCGF, TD2502-110NF, TD2502-110NGF, TD2502-110NDF, TD2502-110NCF, TD2502-110NDGF, TD2502-110NDCF, TD2502-110NCGF, TD2502-110NDCGF, TD2502-110NXF, TD2502-110NXGF, TD2502-110NDXF, TD2502-110NXCF, TD2502-110NDXGF, TD2502-110NDXCF ,TD2502-110NXCGF, TD2502-110NDXCGF, TD2602NF, TD2602N