FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

HAMILTON-C3

K Number: K201306 · Decision Feb 5, 2021
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
30
Review Days
266

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Basic Information

Device Name
HAMILTON-C3
K Number
K201306
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hamilton Medical AG
Date Received
May 15, 2020
Decision Date
February 5, 2021
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.

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Other Clearances by Hamilton Medical AG

K Number Device Name
K201658 Hamilton-C6
K193228 Hamilton-G5
K181216 HAMILTON-T1, HAMILTON-C1
K163283 HAMILTON-H900, HAMILTON-BC8010, HAMILTON-BC4010
K161450 HAMILTON-C3
K153046 HAMILTON-MR1
K152029 HAMILTON-H900, HAMILTON-BC8022, HAMILTON-BC4022, HAMILTON-BC8010, HAMILTON-BC4010
K150893 IntelliCuff
K140939 HAMILTON-T1,HAMILTON-C1
K122438 HAMILTON-MR1
Search all 30 clearances from Hamilton Medical AG →