FDA.reportPublic FDA data

510(k) K802920

Device
Inspiron Pulmonary Function Analyzer
Applicant
C.R. BARD, INC.
510(k) number
K802920
Product code
BZC
Decision
Substantially Equivalent (SESE)
Decision date
1981-02-23
Date received
1980-11-18
Regulation
868.1880
Classification name
Calculator, Pulmonary Function Data
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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