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

HARE MODEL 2000 EZ LOADER MODEL 95555

K Number: K962181 · Decision Aug 1, 1996
Classifications
1
FEI Numbers
105
Registration Numbers
105
Same Product Code
49
Applicant Total
5
Review Days
56

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Basic Information

Device Name
HARE MODEL 2000 EZ LOADER MODEL 95555
K Number
K962181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6910
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dyna Corp.
Date Received
June 6, 1996
Decision Date
August 1, 1996
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 Dyna Corp.

K Number Device Name
K972528 DYNA GLIDE 2600 ROLL-IN AMBULANCE COT (95759)
K902503 HARE FOLDING BACK EMERGENCY STRETCHER
K900670 HARE EMERGENCY STRETCHER
K900671 HARE EMERGENCY STRETCHER WITH WHEELS