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

Panther 5

K Number: K213098 · Decision Jul 20, 2023
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
1
Review Days
664

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Basic Information

Device Name
Panther 5
K Number
K213098
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Origin Medical Devices
Date Received
September 24, 2021
Decision Date
July 20, 2023
Product Code
CBK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CBK Ventilator, Continuous, Facility Use

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