FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ELECTRONIC THERMOMETERS
K Number: K940686
·
Decision Jul 8, 1994
Classifications
1
FEI Numbers
488
Registration Numbers
488
Same Product Code
797
Applicant Total
39
Review Days
142
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Basic Information
- Device Name
- ELECTRONIC THERMOMETERS
- K Number
- K940686
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.2910
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- American Diagnostic Corp.
- Date Received
- February 16, 1994
- Decision Date
- July 8, 1994
- Product Code
- FLL
- 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 |
|---|---|---|---|
| FLL | Continuous Measurement Thermometer | FDA class 2 | General Hospital |
Similar 510(k) Clearances
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| K962655 | ANEROID AND MERCURIAL SPHYGMOMANOMETERS | Jan 27, 1997 | Substantially Equivalent |
| K935944 | PROSCOPES AND ADSCOPES | Mar 3, 1994 | Substantially Equivalent |
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| K894169 | BIOTEL MICROALBUMINURIA (TM) | Sep 18, 1989 | Substantially Equivalent |
| K893608 | ACTICHROME ATIII KIT | Jun 23, 1989 | Substantially Equivalent |
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