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

PEEP VALVE

K Number: K820404 · Decision Mar 1, 1982
Classifications
1
FEI Numbers
71
Registration Numbers
72
Same Product Code
79
Applicant Total
75
Review Days
17

Basic Information

Device Name
PEEP VALVE
K Number
K820404
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5965
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
VITAL SIGNS, INC.
Date Received
February 12, 1982
Decision Date
March 1, 1982
Product Code
BYE
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
BYE Attachment, Breathing, Positive End Expiratory Pressure

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