FDA 510(k)
Substantially Equivalent
🇺🇸 United States
HALL ARTHROTOME
K Number: K832816
·
Decision Nov 28, 1983
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
36
Review Days
101
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Basic Information
- Device Name
- HALL ARTHROTOME
- K Number
- K832816
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- American Sterilizer Co.
- Date Received
- August 19, 1983
- Decision Date
- November 28, 1983
- Advisory Committee
- Unknown
- Review Advisory Committee
- SU
- Third Party
- N
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