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

WALKING AID

K Number: K770608 · Decision Apr 8, 1977
Classifications
1
FEI Numbers
340
Registration Numbers
340
Same Product Code
13
Applicant Total
14
Review Days
8

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Basic Information

Device Name
WALKING AID
K Number
K770608
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3825
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Will Ross Co.
Date Received
March 31, 1977
Decision Date
April 8, 1977
Product Code
ITJ
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
ITJ Walker, Mechanical

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K Number Device Name
K780850 SEARLE NEONATAL OXYGEN PROBE
K771561 DOVER URINE METER
K771132 KENWOOD BIOLOGICAL STEOILIZ. INDICATOR
K770611 PARALLEL BARS
K770612 SPLINT, BOHLER
K770607 TRACTION HARNESS
K770610 TABLE, TREATMENT & TRACTION, HI-LO
K770609 TABLE, MASSAGE & TREATMHNT, FIXED HEIGHT
K770509 TABLE, MASSAGE AND TREATMENT
K770399 VALVE FOR CLOSED SYS. URINARY DRAINAGE
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