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

Amplatzer Talisman Delivery Sheath

K Number: K212738 · Decision Sep 27, 2021
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
44
Review Days
28

Basic Information

Device Name
Amplatzer Talisman Delivery Sheath
K Number
K212738
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abbott Medical
Date Received
August 30, 2021
Decision Date
September 27, 2021
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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