FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PORTA-RESP MONITOR
K Number: K943146
·
Decision Nov 28, 1994
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
4
Review Days
151
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Basic Information
- Device Name
- PORTA-RESP MONITOR
- K Number
- K943146
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.2600
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- S & M Instrument Co.
- Date Received
- June 30, 1994
- Decision Date
- November 28, 1994
- Product Code
- CAP
- 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 |
|---|---|---|---|
| CAP | Monitor, Airway Pressure (Includes Gauge And/Or Alarm) | FDA class 2 | Anesthesiology |
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