FDA 510(k)
FDA unclassified
Substantially Equivalent
🇺🇸 United States
BPA, BODY POSITION ALARM
K Number: K902669
·
Decision Jul 27, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
1
Review Days
39
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Basic Information
- Device Name
- BPA, BODY POSITION ALARM
- K Number
- K902669
- Device Class
- FDA unclassified
- Clearance Type
- Traditional
- Medical Specialty
- Unknown
- Decision
- Substantially Equivalent
- Applicant
- Bagrad
- Date Received
- June 18, 1990
- Decision Date
- July 27, 1990
- Product Code
- LZW
- Advisory Committee
- Unknown
- Review Advisory Committee
- PM
- 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 |
|---|---|---|---|
| LZW | Monitor, Spine Curvature | FDA unclassified | Unknown |
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