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

VITALOGRAPH-ALPHA

K Number: K873562 · Decision Aug 29, 1988
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
17
Review Days
362

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Basic Information

Device Name
VITALOGRAPH-ALPHA
K Number
K873562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vitalograph , Ltd.
Date Received
September 2, 1987
Decision Date
August 29, 1988
Product Code
BZG
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
BZG Spirometer, Diagnostic

Similar 510(k) Clearances

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

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Other Clearances by Vitalograph , Ltd.

K Number Device Name
K253293 VitaloJAK Clinic (Model 7100)
K950854 VITALOGRAPH 2110 SOFTWARE INTERFACE
K925085 ESCORT SPIROMETER
K930085 VITALOGRAPH DATA STORAGE SPIROMETER
K912412 VITALOGRAPH SPIROTRAC III
K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
Search all 17 clearances from Vitalograph , Ltd. →