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

EasyPath RF Introducer Sheath

K Number: K200702 · Decision Jan 14, 2021
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
7
Review Days
302

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Basic Information

Device Name
EasyPath RF Introducer Sheath
K Number
K200702
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Broncus Medical, Inc.
Date Received
March 18, 2020
Decision Date
January 14, 2021
Product Code
EOQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EOQ Bronchoscope (Flexible Or Rigid)

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K183240 Empower RF Catheter
K133385 LUNGPOINT ATV PLANNING AND NAVIGATION SOFTWARE
K131234 LUNGPOINT TOOLS (LUNGPOINT SHEATH, LUNGPOINT DILATION BALLOON)