FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PEEP FACE MASK

K Number: K801883 · Decision Sep 9, 1980
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
54
Applicant Total
75
Review Days
33

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Basic Information

Device Name
PEEP FACE MASK
K Number
K801883
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5580
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Vital Signs, Inc.
Date Received
August 7, 1980
Decision Date
September 9, 1980
Product Code
BYG
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
BYG Mask, Oxygen

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Other Clearances by Vital Signs, Inc.

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K112902 ENFLOW IV FLUID WARMER
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K022402 DISPOSABLE PRESSURE MANOMETER
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
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