FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Y-ADAPTER W/THOUY BORST
K Number: K895580
·
Decision Apr 30, 1990
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
7
Review Days
227
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Basic Information
- Device Name
- Y-ADAPTER W/THOUY BORST
- K Number
- K895580
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1340
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Angeion Corp.
- Date Received
- September 15, 1989
- Decision Date
- April 30, 1990
- Product Code
- DYB
- 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 |
|---|---|---|---|
| DYB | Introducer, Catheter | FDA class 2 | Cardiovascular |
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Other Clearances by Angeion Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K921757 | ANGEION IGITAL ANGEFLATOR | Mar 18, 1993 | Substantially Equivalent |
| K925533 | ANGESTAT(R) PERICARDIAL DRAINAGE SHEATH SET | Jan 12, 1993 | Substantially Equivalent |
| K915719 | ANGEION ENDOSCOPIC VALVE SEAL | Feb 18, 1992 | Substantially Equivalent |
| K902377 | ANGEFLATOR(TM) | Dec 13, 1990 | Substantially Equivalent |
| K894446 | ANGEION HEMOSTASIS VALVE INTRODUCER | Nov 30, 1989 | Substantially Equivalent |
| K871153 | CATHETER INTRODUCER | Jun 24, 1987 | Substantially Equivalent |