FDA 510(k)
Substantially Equivalent
🇺🇸 United States
CYBREX PHENOBARBITAL
K Number: K801566
·
Decision Jul 21, 1980
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
883
Review Days
13
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Basic Information
- Device Name
- CYBREX PHENOBARBITAL
- K Number
- K801566
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Abbott Laboratories
- Date Received
- July 8, 1980
- Decision Date
- July 21, 1980
- Advisory Committee
- Unknown
- Review Advisory Committee
- TX
- Third Party
- N
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