FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MEDICON #8200 AMS
K Number: K812873
·
Decision Nov 16, 1981
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
174
Applicant Total
14
Review Days
33
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Basic Information
- Device Name
- MEDICON #8200 AMS
- K Number
- K812873
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2375
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Medicon, Inc.
- Date Received
- October 14, 1981
- Decision Date
- November 16, 1981
- Product Code
- BZQ
- 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 |
|---|---|---|---|
| BZQ | Monitor, Breathing Frequency | FDA class 2 | Anesthesiology |
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