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

FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, A14007, A14008

K Number: K010838 · Decision Jun 21, 2001
Classifications
1
FEI Numbers
276
Registration Numbers
277
Same Product Code
889
Applicant Total
3
Review Days
93

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Basic Information

Device Name
FOX PTA CATHETER, 3.0, 4.0, 5.0, 6.0, 7.0, AND 8.0 X 40 MM, MODELS A14003, A14004, A14005, A14006, A14007, A14008
K Number
K010838
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Jomed AG
Date Received
March 20, 2001
Decision Date
June 21, 2001
Product Code
DQY
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
DQY Catheter, Percutaneous

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Other Clearances by Jomed AG

K Number Device Name
K030053 JOSTENT SELFX, MODELS 015SX4406; 015SX4408; 015SX4410; 015SX680; 015SX6808; 015SX6810
K020854 MODIFICATION TO FOX PTA CATHETER