FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
NIPRO NEEDLELESS TRANSFER DEVICE, MODELS: M285503 AND M285505
K Number: K092246
·
Decision Nov 12, 2009
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
205
Applicant Total
34
Review Days
107
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Basic Information
- Device Name
- NIPRO NEEDLELESS TRANSFER DEVICE, MODELS: M285503 AND M285505
- K Number
- K092246
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Nipro Medical Corporation
- Date Received
- July 28, 2009
- Decision Date
- November 12, 2009
- Product Code
- LHI
- 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 |
|---|---|---|---|
| LHI | Set, I.V. Fluid Transfer | FDA class 2 | General Hospital |
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