FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CHASE TWO STAGE VENOUS RETURN CATHETER
K Number: K964195
·
Decision Mar 19, 1997
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
393
Applicant Total
27
Review Days
149
Basic Information
- Device Name
- CHASE TWO STAGE VENOUS RETURN CATHETER
- K Number
- K964195
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4210
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- CHASE MEDICAL, INC.
- Date Received
- October 21, 1996
- Decision Date
- March 19, 1997
- Product Code
- DWF
- 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 |
|---|---|---|---|
| DWF | Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass | FDA class 2 | Cardiovascular |
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Other Clearances by CHASE MEDICAL, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K032531 | CHASE CARDIAC ANALYSIS SYSTEM | Feb 2, 2004 | Substantially Equivalent |
| K022093 | CHASE CARDIOVASCULAR PATCH KIT | Sep 20, 2002 | Substantially Equivalent |
| K021129 | CHARE CARIOVASCULAR PATCH | Jun 3, 2002 | Substantially Equivalent |
| K020233 | CHASE CARDIOVASCULAR PATCH KIT | Mar 14, 2002 | Substantially Equivalent |
| K020132 | CHASE CARDIOVASCULAR PATCH KIT | Feb 26, 2002 | Substantially Equivalent |
| K012248 | CHASE CARDIOVASCULAR PATCH | Aug 10, 2001 | Substantially Equivalent |
| K003467 | CHASE CARDIOVASCULAR PATCH | Jan 29, 2001 | Substantially Equivalent |
| K001662 | CHASE CARDIOVASCULAR PATCH | Aug 2, 2000 | Substantially Equivalent |
| K972993 | CHASE FEMORAL ACCESS CANNULATION SET | Mar 31, 1998 | Substantially Equivalent |
| K974568 | CHASE ANASTOMOSIS VISUALIZATION DEVICE | Jan 6, 1998 | Substantially Equivalent |