FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE
K Number: K883174
·
Decision Oct 14, 1988
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
503
Review Days
79
Basic Information
- Device Name
- MULTI-MED INFUSION CATHETER AND KIT DOUBLE/TRIPLE
- K Number
- K883174
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- BAXTER HEALTHCARE CORP.
- Date Received
- July 27, 1988
- Decision Date
- October 14, 1988
- Product Code
- DQY
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQY | Catheter, Percutaneous | FDA class 2 | Cardiovascular |
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