FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MICRO MEDICAL DATA SYSTEM
K Number: K800241
·
Decision Feb 26, 1980
Classifications
1
FEI Numbers
115
Registration Numbers
116
Same Product Code
77
Applicant Total
2
Review Days
21
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Basic Information
- Device Name
- MICRO MEDICAL DATA SYSTEM
- K Number
- K800241
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 862.2100
- Medical Specialty
- Clinical Chemistry
- Decision
- Substantially Equivalent
- Applicant
- Micro/Tel., Inc.
- Date Received
- February 5, 1980
- Decision Date
- February 26, 1980
- Product Code
- JQP
- Advisory Committee
- Clinical Chemistry
- Review Advisory Committee
- CH
- 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 |
|---|---|---|---|
| JQP | Calculator/Data Processing Module, For Clinical Use | FDA class 1 | Clinical Chemistry |
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Other Clearances by Micro/Tel., Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K800242 | MICRO MEDICAL DATA SYSTEM II | Mar 3, 1980 | Substantially Equivalent |