FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MR Conditional CGA 870
K Number: K162811
·
Decision Mar 2, 2017
Classifications
1
FEI Numbers
111
Registration Numbers
112
Same Product Code
54
Applicant Total
4
Review Days
147
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Basic Information
- Device Name
- MR Conditional CGA 870
- K Number
- K162811
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.2700
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Essex Industries, Inc.
- Date Received
- October 6, 2016
- Decision Date
- March 2, 2017
- 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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