FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SAFECIRCUIT MANIFOLD/PULMONARY UNIT
K Number: K953269
·
Decision Dec 20, 1996
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
42
Applicant Total
3
Review Days
526
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Basic Information
- Device Name
- SAFECIRCUIT MANIFOLD/PULMONARY UNIT
- K Number
- K953269
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5430
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Advanced Warming Systems, Inc.
- Date Received
- July 13, 1995
- Decision Date
- December 20, 1996
- Product Code
- CBN
- 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 |
|---|---|---|---|
| CBN | Apparatus, Gas-Scavenging | FDA class 2 | Anesthesiology |
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