FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
INFUSION FLUID WARMER
K Number: K883873
·
Decision Feb 28, 1989
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
74
Applicant Total
20
Review Days
168
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Basic Information
- Device Name
- INFUSION FLUID WARMER
- K Number
- K883873
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Pmt Corp.
- Date Received
- September 13, 1988
- Decision Date
- February 28, 1989
- Product Code
- LGZ
- 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 |
|---|---|---|---|
| LGZ | Warmer, Thermal, Infusion Fluid | FDA class 2 | General Hospital |
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