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

SPIROMED RESPIROMETER

K Number: K831237 · Decision May 9, 1983
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
78
Review Days
24

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Basic Information

Device Name
SPIROMED RESPIROMETER
K Number
K831237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1850
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Draeger Medical, Inc.
Date Received
April 15, 1983
Decision Date
May 9, 1983
Product Code
BZK
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZK Spirometer, Monitoring (W/Wo Alarm)

Similar 510(k) Clearances

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

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Other Clearances by Draeger Medical, Inc.

K Number Device Name
K042607 PRIMUS US
K042419 FABIUS GS/FABIUS TIRO ANESTHESIA SYSTEM
K042276 D-VAPOR
K042086 FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM
K041622 MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM; FABIUS TIRO ANESTHESIA SYSTEM
K040847 MODIFICATION TO VAMOS ANESTHETIC GAS MONITOR
K033498 NARKOMED 6400, MODEL NM6400
K030624 MODIFICATION TO FABIUS GS ANESTHESIA SYSTEM
K031400 FABIUS TIRO ANESTHESIA SYSTEM
K022031 NARKOMED MRI-2 ANESTHESIA SYSTEM, MODEL NM-MRI-2
Search all 78 clearances from Draeger Medical, Inc. →