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

Recon Support Catheter

K Number: K203275 · Decision Mar 1, 2021
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
31
Review Days
115

Basic Information

Device Name
Recon Support Catheter
K Number
K203275
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
C.R. Bard, Inc.
Date Received
November 6, 2020
Decision Date
March 1, 2021
Product Code
DQY
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

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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