FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
OSADA ENDEX
K Number: K904742
·
Decision Dec 17, 1990
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
45
Applicant Total
3
Review Days
60
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Basic Information
- Device Name
- OSADA ENDEX
- K Number
- K904742
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Osada Electric Co., Ltd.
- Date Received
- October 18, 1990
- Decision Date
- December 17, 1990
- Product Code
- LQY
- Advisory Committee
- Unknown
- Review Advisory Committee
- DE
- 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 |
|---|---|---|---|
| LQY | Locator, Root Apex | FDA unclassified | Unknown |
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