FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POSID SAMPLER
K Number: K860508
·
Decision May 2, 1986
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
130
Review Days
80
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Basic Information
- Device Name
- POSID SAMPLER
- K Number
- K860508
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2750
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Organon Teknika Corp.
- Date Received
- February 11, 1986
- Decision Date
- May 2, 1986
- Product Code
- JQW
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JQW | Station, Pipetting And Diluting, For Clinical Use | FDA class 1 | Clinical Chemistry |
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| K993576 | BACT/ALERT MP PROCESS BOTTLE | Dec 14, 1999 | Substantially Equivalent |
| K992432 | BACT/ALERT FN | Sep 24, 1999 | Substantially Equivalent |
| K983762 | NUCLISENS CMV PP67 | Sep 15, 1999 | Substantially Equivalent |
| K992401 | BACT/ALERT PF | Sep 3, 1999 | Substantially Equivalent |