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

PERAMBULATOR (STROLLER)

K Number: K862888 · Decision Aug 13, 1986
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
7
Applicant Total
12
Review Days
22

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Basic Information

Device Name
PERAMBULATOR (STROLLER)
K Number
K862888
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3850
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Mednet, Inc.
Date Received
July 22, 1986
Decision Date
August 13, 1986
Product Code
LBE
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
LBE Stroller, Adaptive

Similar 510(k) Clearances

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Other Clearances by Mednet, Inc.

K Number Device Name
K955782 MED-NET STOPCOCKS
K862887 UPHOLSTERED BUCKET SEAT
K862883 ORTHOPEDIC SEATS
K862885 CAR SEAT
K862892 CASTER CAR
K862895 TRICYCLES
K862893 VENTRAL STANDING UNIT
K862894 SCHOOLTABLE
K862889 KIRO, WHEELCHAIR FOR CHILDREN
K862890 TOILET/SHOWER CHAIR
Search all 12 clearances from Mednet, Inc. →