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

MOBILIZER

K Number: K840551 · Decision Mar 23, 1984
Classifications
1
FEI Numbers
248
Registration Numbers
248
Same Product Code
42
Applicant Total
8
Review Days
44

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Basic Information

Device Name
MOBILIZER
K Number
K840551
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.5370
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Lossing Orthopedic, Inc.
Date Received
February 8, 1984
Decision Date
March 23, 1984
Product Code
ION
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
ION Exerciser, Non-Measuring

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K823236 BACK ON TRACK INVERSION THERAPY & EXER
K813017 NECKTRAC
K802555 COTTRELL 90/90 BACKTRAC