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

SUREBREATH DOME, E-Z BREATHER

K Number: K915158 · Decision Feb 12, 1992
Classifications
1
FEI Numbers
656
Registration Numbers
656
Same Product Code
99
Applicant Total
18
Review Days
90

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Basic Information

Device Name
SUREBREATH DOME, E-Z BREATHER
K Number
K915158
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ipax, Inc.
Date Received
November 14, 1991
Decision Date
February 12, 1992
Product Code
GAD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GAD Retractor

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Other Clearances by Ipax, Inc.

K Number Device Name
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K971245 BLINK EXTERNAL EYELID WEIGHT
K915118 PHACO EMULSIFICATION,IRRIGATION/ASPIRATION TUBE
K914172 KPE 230 AM
K914221 KPE 220 TS, NONSTERILE
K884076 SUREBREATH DOME
K873097 PROCEDUAL CHANGES/ASSEMBLY PROCESS FOR PLUS PAKS
K870770 TIMLEINE(TM) VENIPUNCTURE SYSTEM
K864726 I/A/KPE TIP
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