FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

DATEX ENGSTOM MANUAL RESUSCITATOR

K Number: K970991 · Decision Jun 16, 1997
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
208
Applicant Total
16
Review Days
89

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Basic Information

Device Name
DATEX ENGSTOM MANUAL RESUSCITATOR
K Number
K970991
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5915
Medical Specialty
Anesthesiology
Decision
Unknown
Statement or Summary
Summary
Applicant
Promedic, Inc.
Date Received
March 19, 1997
Decision Date
June 16, 1997
Product Code
BTM
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
BTM Ventilator, Emergency, Manual (Resuscitator)

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K060842 REVJET TURBO
K052903 PEDIATRIC FEEDING TUBE
K031409 URINARY CATHETERS
K024190 FENESTRATED INFUSION CATHETER
K023579 GAS SAMPLING LINES
K020005 INFANT FEEDING TUBES
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