FDA 510(k)
Unknown
🇺🇸 United States
REGULATOR VENOSET W/0.22 MICRON IVEX
K Number: K810029
·
Decision Jan 6, 1981
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
883
Review Days
—
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Basic Information
- Device Name
- REGULATOR VENOSET W/0.22 MICRON IVEX
- K Number
- K810029
- Clearance Type
- Traditional
- Decision
- Unknown
- Applicant
- Abbott Laboratories
- Date Received
- January 6, 1981
- Decision Date
- January 6, 1981
- Advisory Committee
- Unknown
- Review Advisory Committee
- HO
- Third Party
- N
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