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

CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF)

K Number: K121398 · Decision Dec 13, 2012
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
1
Review Days
218

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Basic Information

Device Name
CHARLIE GUIDEWIRE (REGULAR), CHARLIE GUIDEWIRE (STIFF)
K Number
K121398
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1330
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Guidepath Medical, Inc.
Date Received
May 9, 2012
Decision Date
December 13, 2012
Product Code
DQX
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
DQX Wire, Guide, Catheter

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