FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ARI STANDARD ANESTHESIA RECORD
K Number: K854213
·
Decision Dec 19, 1985
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
187
Applicant Total
30
Review Days
63
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Basic Information
- Device Name
- ARI STANDARD ANESTHESIA RECORD
- K Number
- K854213
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5160
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Agilent Technologies, Inc.
- Date Received
- October 17, 1985
- Decision Date
- December 19, 1985
- Product Code
- BSZ
- 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 |
|---|---|---|---|
| BSZ | Gas-Machine, Anesthesia | FDA class 2 | Anesthesiology |
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