FDA 510(k)
Substantially Equivalent
🇺🇸 United States
DIAGNOSTICS HDL CHOLESTEROL PRECIPITANT
K Number: K821852
·
Decision Jul 2, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
340
Review Days
9
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Basic Information
- Device Name
- DIAGNOSTICS HDL CHOLESTEROL PRECIPITANT
- K Number
- K821852
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Boehringer Mannheim Corp.
- Date Received
- June 23, 1982
- Decision Date
- July 2, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- CH
- Third Party
- N
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