FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
IQ UREA NITROGEN
K Number: K863901
·
Decision Nov 24, 1986
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
10
Applicant Total
632
Review Days
48
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Basic Information
- Device Name
- IQ UREA NITROGEN
- K Number
- K863901
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 862.1770
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Date Received
- October 7, 1986
- Decision Date
- November 24, 1986
- Product Code
- JGZ
- 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 |
|---|---|---|---|
| JGZ | O-Phthalaldehyde, Urea Nitrogen | FDA class 2 | Clinical Chemistry |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (JGZ), ordered by most recent decision date.
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