510(k) K222525

Device
Alveoair Digital Spirometer
Applicant
Roundworks Technologies Private Limited
510(k) number
K222525
Product code
BZG
Decision
Substantially Equivalent (SESE)
Decision date
2023-08-28
Date received
2022-08-22
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
Prashant Patel
Address
Office # B 302, Bldg. # B, 3rd Floor, Go Sq., Survey #249/250, Above Surya Electronic Wakad, Pune IN 411047 411047

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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