FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE
K Number: K872182
·
Decision Oct 30, 1987
Classifications
1
FEI Numbers
271
Registration Numbers
272
Same Product Code
880
Applicant Total
8
Review Days
144
Basic Information
- Device Name
- POLYSTAN WIRE REINFORCED CATHETERS AND CANNULAE
- K Number
- K872182
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1250
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- POLYSTAN C/O VITALCOR, INC.
- Date Received
- June 8, 1987
- Decision Date
- October 30, 1987
- 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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Other Clearances by POLYSTAN C/O VITALCOR, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K894657 | POLYSTAN HEART-LUNG MACHINE SYSTEM | Mar 28, 1990 | Substantially Equivalent |
| K893940 | POLYSTAN HEATER-COOLER UNIT | Jan 18, 1990 | Substantially Equivalent |
| K893704 | SAFE-1 | Dec 22, 1989 | Substantially Equivalent |
| K893705 | SAFE-1 VENOUS RESERVOIR | Dec 22, 1989 | Substantially Equivalent |
| K874853 | POLYSTAN TWO STAGE CATHETERS | Feb 5, 1988 | Substantially Equivalent |
| K874852 | POLYSTAN WIRE REINFORCED TWO STAGE CATHETERS | Feb 5, 1988 | Substantially Equivalent |
| K843538 | PO 2 LYTRODE | Oct 18, 1984 | Substantially Equivalent |