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

MULLINS-X, MODEL 250X

K Number: K082868 · Decision Oct 24, 2008
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
44
Review Days
25

Basic Information

Device Name
MULLINS-X, MODEL 250X
K Number
K082868
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NUMED, INC.
Date Received
September 29, 2008
Decision Date
October 24, 2008
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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