FDA 510(k)
Substantially Equivalent
🇺🇸 United States
NEOSERV 824
K Number: K900729
·
Decision Jun 8, 1990
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
38
Review Days
113
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Basic Information
- Device Name
- NEOSERV 824
- K Number
- K900729
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Burdick Corp.
- Date Received
- February 15, 1990
- Decision Date
- June 8, 1990
- Product Code
- MCJ
- Advisory Committee
- Unknown
- Review Advisory Committee
- OR
- Third Party
- N
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