FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ROTATING HEMOSTATIC VALVE
K Number: K890800
·
Decision Jun 12, 1989
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
402
Applicant Total
136
Review Days
116
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Basic Information
- Device Name
- ROTATING HEMOSTATIC VALVE
- K Number
- K890800
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Datascope Corp.
- Date Received
- February 16, 1989
- Decision Date
- June 12, 1989
- Product Code
- LIT
- 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 |
|---|---|---|---|
| LIT | Catheter, Angioplasty, Peripheral, Transluminal | FDA class 2 | Cardiovascular |
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