FDA 510(k)
Substantially Equivalent
🇺🇸 United States
EXTRACTOR III
K Number: K820292
·
Decision Mar 2, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
60
Review Days
27
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Basic Information
- Device Name
- EXTRACTOR III
- K Number
- K820292
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- The Anspach Effort, Inc.
- Date Received
- February 3, 1982
- Decision Date
- March 2, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
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