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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