FDA 510(k)
Substantially Equivalent
🇺🇸 United States
SIMPLAMATIC III
K Number: K827450
·
Decision May 19, 1982
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
9
Review Days
22
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Basic Information
- Device Name
- SIMPLAMATIC III
- K Number
- K827450
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Spectrum X-Ray Corp.
- Date Received
- April 27, 1982
- Decision Date
- May 19, 1982
- Advisory Committee
- Unknown
- Review Advisory Committee
- RA
- Third Party
- N
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