FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
# 10099/10225/10235/10275/10525/10625/10715/10125
K Number: K862193
·
Decision Jul 9, 1986
Classifications
1
FEI Numbers
111
Registration Numbers
112
Same Product Code
54
Applicant Total
3
Review Days
30
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Basic Information
- Device Name
- # 10099/10225/10235/10275/10525/10625/10715/10125
- K Number
- K862193
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.2700
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- U.O. Equipment Co.
- Date Received
- June 9, 1986
- Decision Date
- July 9, 1986
- Product Code
- CAN
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| CAN | Regulator, Pressure, Gas Cylinder | FDA class 1 | Anesthesiology |
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