FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BD ECLIPSE BIFURCATED NEEDLE
K Number: K032528
·
Decision Sep 9, 2003
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
24
Applicant Total
190
Review Days
25
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Basic Information
- Device Name
- BD ECLIPSE BIFURCATED NEEDLE
- K Number
- K032528
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 880.5570
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Becton, Dickinson & CO
- Date Received
- August 15, 2003
- Decision Date
- September 9, 2003
- Product Code
- SCL
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| SCL | Allergen And Vaccine Delivery Needles | FDA class 2 | General Hospital |
Similar 510(k) Clearances
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