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

EndoTool IV 1.10

K Number: K200443 · Decision Mar 17, 2020
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
54
Applicant Total
3
Review Days
22

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Basic Information

Device Name
EndoTool IV 1.10
K Number
K200443
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1890
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Monarch Medical Technologies, LLC
Date Received
February 24, 2020
Decision Date
March 17, 2020
Product Code
NDC
Advisory Committee
Anesthesiology
Review Advisory Committee
CH
Third Party
Y

Classifications

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

Product Code Device Name
NDC Calculator, Drug Dose

Similar 510(k) Clearances

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

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Other Clearances by Monarch Medical Technologies, LLC

K Number Device Name
K211160 EndoTool SubQ 2.1
K201619 EndoTool IV System