FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BITE BLOCK #59430
K Number: K890567
·
Decision Feb 17, 1989
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
27
Applicant Total
4
Review Days
11
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Basic Information
- Device Name
- BITE BLOCK #59430
- K Number
- K890567
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5070
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Applicant
- Medi-Source, Inc.
- Date Received
- February 6, 1989
- Decision Date
- February 17, 1989
- Product Code
- JXL
- 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 |
|---|---|---|---|
| JXL | Block, Bite | FDA class 2 | Neurology |
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