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

BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER

K Number: K863083 · Decision Sep 3, 1986
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
49
Applicant Total
2
Review Days
22

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Basic Information

Device Name
BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER
K Number
K863083
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Beta Medical Products Co.
Date Received
August 12, 1986
Decision Date
September 3, 1986
Product Code
FPO
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
FPO Stretcher, Wheeled

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Other Clearances by Beta Medical Products Co.

K Number Device Name
K884531 BETA 90/50 MOBILE IMAGING TABLE