FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RATEMINDER II SPECIALTY CARE
K Number: K833520
·
Decision Dec 22, 1983
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
59
Applicant Total
2
Review Days
72
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Basic Information
- Device Name
- RATEMINDER II SPECIALTY CARE
- K Number
- K833520
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5725
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Applicant
- Anatros Corp.
- Date Received
- October 11, 1983
- Decision Date
- December 22, 1983
- Product Code
- LDR
- 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 |
|---|---|---|---|
| LDR | Controller, Infusion, Intravascular, Electronic | FDA class 2 | General Hospital |
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Other Clearances by Anatros Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K812233 | RATEMINDER | Aug 25, 1981 | Substantially Equivalent |