FDA 510(k)
Substantially Equivalent
🇺🇸 United States
DIAGNOSTIC MICROSOPCE SLIDES
K Number: K844092
·
Decision Oct 25, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
37
Review Days
6
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Basic Information
- Device Name
- DIAGNOSTIC MICROSOPCE SLIDES
- K Number
- K844092
- Clearance Type
- Traditional
- Decision
- Substantially Equivalent
- Applicant
- Sybron Corp.
- Date Received
- October 19, 1984
- Decision Date
- October 25, 1984
- Advisory Committee
- Unknown
- Review Advisory Committee
- CH
- Third Party
- N
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