FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ANETHESIA BREATHING CIRCUIT
K Number: K895357
·
Decision Oct 19, 1989
Classifications
1
FEI Numbers
199
Registration Numbers
199
Same Product Code
183
Applicant Total
4
Review Days
52
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Basic Information
- Device Name
- ANETHESIA BREATHING CIRCUIT
- K Number
- K895357
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 868.5240
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- F.L.W. Plastics, Inc.
- Date Received
- August 28, 1989
- Decision Date
- October 19, 1989
- Product Code
- CAI
- 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 |
|---|---|---|---|
| CAI | Circuit, Breathing (W Connector, Adaptor, Y Piece) | FDA class 1 | Anesthesiology |
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