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

SAFERSLEEP SYSTEM

K Number: K050883 · Decision Nov 4, 2005
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
1
Review Days
211

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Basic Information

Device Name
SAFERSLEEP SYSTEM
K Number
K050883
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5160
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Safer Sleep, LLC
Date Received
April 7, 2005
Decision Date
November 4, 2005
Product Code
BSZ
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
BSZ Gas-Machine, Anesthesia

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