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

PnueAira (PNCU-01)

K Number: K251086 · Decision Aug 18, 2025
Classifications
1
FEI Numbers
129
Registration Numbers
129
Same Product Code
349
Applicant Total
1
Review Days
131

Basic Information

Device Name
PnueAira (PNCU-01)
K Number
K251086
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biotab, LLC
Date Received
April 9, 2025
Decision Date
August 18, 2025
Product Code
JOW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

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

Product Code Device Name
JOW Sleeve, Limb, Compressible

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