FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR
K Number: K850394
·
Decision Apr 24, 1985
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
14
Review Days
82
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Basic Information
- Device Name
- LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR
- K Number
- K850394
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.4500
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Vascutech, Inc.
- Date Received
- February 1, 1985
- Decision Date
- April 24, 1985
- Product Code
- DWS
- 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 |
|---|---|---|---|
| DWS | Instruments, Surgical, Cardiovascular | FDA class 1 | Cardiovascular |
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Other Clearances by Vascutech, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K001621 | DARDIK CAROTID SHUNT | Dec 6, 2000 | Substantially Equivalent |
| K992942 | LEMAITRE OCCLUSION CATHETER | Apr 13, 2000 | Substantially Equivalent |
| K992933 | LEMAITRE IRRIGATION CATHETER | Mar 8, 2000 | Substantially Equivalent |
| K992934 | LEMAITRE VENOUS THROMBECTOMY CATHETER | Mar 1, 2000 | Substantially Equivalent |
| K992940 | LEMAITRE BALLOON CATHETER WITH IRRIGATION | Feb 22, 2000 | Substantially Equivalent |
| K992941 | LEMAITRE BILIARY CATHETER | Jan 12, 2000 | Substantially Equivalent |
| K992368 | LEMAITRE EMBOLECTOMY CATHETER | Dec 9, 1999 | Substantially Equivalent |
| K980723 | 2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT) | Feb 12, 1999 | Substantially Equivalent |
| K946352 | LEMAITRE VALVULOTOME II | Jun 21, 1995 | Substantially Equivalent |
| K932009 | THE SAMUELS RETROGRAD VALVULOTOME | Sep 21, 1993 | Substantially Equivalent |