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

CLIRPATH TURBO EXCIMER LASER CATHETERS

K Number: K052296 · Decision Sep 2, 2005
Classifications
1
FEI Numbers
42
Registration Numbers
42
Same Product Code
56
Applicant Total
24
Review Days
10

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Basic Information

Device Name
CLIRPATH TURBO EXCIMER LASER CATHETERS
K Number
K052296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectranetics Corp.
Date Received
August 23, 2005
Decision Date
September 2, 2005
Product Code
PDU
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
PDU Catheter For Crossing Total Occlusions

Similar 510(k) Clearances

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

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Other Clearances by Spectranetics Corp.

K Number Device Name
K140047 LEXICONTURE MECHANICAL DILATOR SHEATH SET
K123632 2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035
K112032 8FR TURBO - TANDEM SYSTEM
K093257 TORQMAX SHEATH GRIP ACCESSORY
K094036 TURBO-TANDEM SYSTEM MODEL 472-110
K092378 SPECTRANETICS VISISHEATH DILATOR SHEATH
K092396 SPECTRANETICS QUICK CROSS EXTREME SUPPORT CATHETERS
K091299 SPECTRANETICS TURBO-TANDEM SYSTEM
K090913 CROSS-PILOT TURBO ELITE SUPPORT CATHETER
K082559 SPECTRANETICS CROSS-PILOT TURBO ELITE SUPPORT CATHETER
Search all 24 clearances from Spectranetics Corp. →