FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SPINOCAN(R) CONTINUOUS SPINAL TRAY
K Number: K895192
·
Decision Sep 18, 1989
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
9
Review Days
38
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Basic Information
- Device Name
- SPINOCAN(R) CONTINUOUS SPINAL TRAY
- K Number
- K895192
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5140
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Burron Medical, Inc.
- Date Received
- August 11, 1989
- Decision Date
- September 18, 1989
- Product Code
- CAZ
- 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 |
|---|---|---|---|
| CAZ | Anesthesia Conduction Kit | FDA class 2 | Anesthesiology |
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