FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
TORQUE DEVICE FOR A GUIDE WIRE
K Number: K910969
·
Decision May 16, 1991
Classifications
1
FEI Numbers
257
Registration Numbers
258
Same Product Code
763
Applicant Total
21
Review Days
71
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Basic Information
- Device Name
- TORQUE DEVICE FOR A GUIDE WIRE
- K Number
- K910969
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1330
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Terumo Corp.
- Date Received
- March 6, 1991
- Decision Date
- May 16, 1991
- Product Code
- DQX
- 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 |
|---|---|---|---|
| DQX | Wire, Guide, Catheter | FDA class 2 | Cardiovascular |
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