FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SCANLAN VASCU-STATT
K Number: K802829
·
Decision Jan 15, 1981
Classifications
1
FEI Numbers
374
Registration Numbers
374
Same Product Code
22
Applicant Total
19
Review Days
66
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Basic Information
- Device Name
- SCANLAN VASCU-STATT
- K Number
- K802829
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.6450
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Scanlan Intl., Inc.
- Date Received
- November 10, 1980
- Decision Date
- January 15, 1981
- Product Code
- FMP
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FMP | Protector, Skin Pressure | FDA class 1 | General Hospital |
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Other Clearances by Scanlan Intl., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K960372 | SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM | Apr 26, 1996 | Substantially Equivalent |
| K945474 | SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER | Dec 5, 1994 | Substantially Equivalent |
| K911184 | SCANLAN/TAHERI VALVULOTOME | Feb 18, 1992 | Substantially Equivalent |
| K864920 | SCANLAN (TM) INSTRUMENT TRAY | Jan 12, 1987 | Substantially Equivalent |
| K864919 | SCANLAN (TM) VEIN/GRAFT HOLDER | Jan 12, 1987 | Substantially Equivalent |
| K851825 | SCANLAN TUNNELER, SHEATH & TIP | Jul 12, 1985 | Substantially Equivalent |
| K841521 | SCANLAN ENDARSECTOR | Aug 3, 1984 | Substantially Equivalent |
| K841513 | SCANLAN ATRAUM INSTRUMENT JAW COVER | Jul 6, 1984 | Substantially Equivalent |
| K841085 | SCANLAN COLORMARK SKIN MARKER | Jun 11, 1984 | Substantially Equivalent |
| K841515 | SCANLAN VASCU-STATT II | Jun 5, 1984 | Substantially Equivalent |