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

TORQMAX SHEATH GRIP ACCESSORY

K Number: K093257 · Decision Mar 26, 2010
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
0
Applicant Total
24
Review Days
158

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Basic Information

Device Name
TORQMAX SHEATH GRIP ACCESSORY
K Number
K093257
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectranetics Corp.
Date Received
October 19, 2009
Decision Date
March 26, 2010
Product Code
OFC
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
OFC Catheter Introducer Kit

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
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
K082561 SPECTRANETICS QUICK-CROSS EXTREME SUPPORT CATHETERS
Search all 24 clearances from Spectranetics Corp. →