510(k) K200550

Device
Vitalograph Model 2120 In2itive eDiary
Applicant
Vitalograph Ireland, Ltd.
510(k) number
K200550
Product code
BZG
Decision
Substantially Equivalent (SESE)
Decision date
2020-07-27
Date received
2020-03-03
Regulation
868.1840
Classification name
Spirometer, Diagnostic
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Tony O'Hanlon
Address
Gort Rd. Business Park Ennis Co Clare IE V95 HFT4 V95 HFT4

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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