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

ESCORT SPIROMETER

K Number: K925085 · Decision Aug 12, 1993
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
227
Applicant Total
17
Review Days
309

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Basic Information

Device Name
ESCORT SPIROMETER
K Number
K925085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1840
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Vitalograph , Ltd.
Date Received
October 7, 1992
Decision Date
August 12, 1993
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

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Other Clearances by Vitalograph , Ltd.

K Number Device Name
K253293 VitaloJAK Clinic (Model 7100)
K950854 VITALOGRAPH 2110 SOFTWARE INTERFACE
K930085 VITALOGRAPH DATA STORAGE SPIROMETER
K912412 VITALOGRAPH SPIROTRAC III
K893665 AEROSOL INHALATION MONITOR
K892524 VITALOGRAPH-BREATHCO MONITOR
K873562 VITALOGRAPH-ALPHA
K874892 VITALOGRAPH-EC60 HYDROGEN MONITOR
K863420 VITALOGRAPH EC-50 CARBON MONOXIDE MONITOR
K860949 DUAL-AID
Search all 17 clearances from Vitalograph , Ltd. →