FDA 510(k) Substantially Equivalent 🇺🇸 United States

ALCYON ROTATIONAL COBALT THERAPY

K Number: K837465 · Decision Jun 28, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
20
Review Days
56

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Basic Information

Device Name
ALCYON ROTATIONAL COBALT THERAPY
K Number
K837465
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Cgr Medical Corp.
Date Received
May 3, 1983
Decision Date
June 28, 1983
Advisory Committee
Unknown
Review Advisory Committee
RA
Third Party
N

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