FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SENTRY SCALE
K Number: K905122
·
Decision Mar 15, 1991
Classifications
1
FEI Numbers
98
Registration Numbers
98
Same Product Code
47
Applicant Total
3
Review Days
121
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Basic Information
- Device Name
- SENTRY SCALE
- K Number
- K905122
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.2720
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Apollo Enterprise, Ltd. Co.
- Date Received
- November 14, 1990
- Decision Date
- March 15, 1991
- Product Code
- FRW
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| FRW | Scale, Patient | FDA class 1 | General Hospital |
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