FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
DIGITCARE I.V. START KIT
K Number: K905009
·
Decision Dec 18, 1990
Classifications
1
FEI Numbers
204
Registration Numbers
205
Same Product Code
503
Applicant Total
3
Review Days
41
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Basic Information
- Device Name
- DIGITCARE I.V. START KIT
- K Number
- K905009
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5200
- Medical Specialty
- General Hospital
- Decision
- Unknown
- Applicant
- Digitcare Corp.
- Date Received
- November 7, 1990
- Decision Date
- December 18, 1990
- Product Code
- FOZ
- 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 |
|---|---|---|---|
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | FDA class 2 | General Hospital |
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