FDA 510(k) Substantially Equivalent 🇺🇸 United States

MYOCATH CATOLOG NO. MCK-A

K Number: K812052 · Decision Oct 6, 1981
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
69
Review Days
77

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Basic Information

Device Name
MYOCATH CATOLOG NO. MCK-A
K Number
K812052
Clearance Type
Traditional
Decision
Substantially Equivalent
Applicant
Sorensen Research
Date Received
July 21, 1981
Decision Date
October 6, 1981
Advisory Committee
Unknown
Review Advisory Committee
PM
Third Party
N

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