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

VACUUM STRETCHER IMMOBILIZER

K Number: K840034 · Decision Feb 27, 1984
Classifications
1
FEI Numbers
124
Registration Numbers
124
Same Product Code
38
Applicant Total
14
Review Days
53

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Basic Information

Device Name
VACUUM STRETCHER IMMOBILIZER
K Number
K840034
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6900
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Medicon, Inc.
Date Received
January 5, 1984
Decision Date
February 27, 1984
Product Code
FPP
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FPP Stretcher, Hand-Carried

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