FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
HILAL EMBOLIZATION MICROCOIL(TM)
K Number: K901337
·
Decision Nov 13, 1990
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
184
Applicant Total
190
Review Days
236
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Basic Information
- Device Name
- HILAL EMBOLIZATION MICROCOIL(TM)
- K Number
- K901337
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5950
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Cook, Inc.
- Date Received
- March 22, 1990
- Decision Date
- November 13, 1990
- Product Code
- HCG
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- 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 |
|---|---|---|---|
| HCG | Device, Neurovascular Embolization | FDA class 2 | Neurology |
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