FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
DUAL HEAD STETHOSCOPE
K Number: K791338
·
Decision Aug 10, 1979
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
153
Applicant Total
6
Review Days
21
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Basic Information
- Device Name
- DUAL HEAD STETHOSCOPE
- K Number
- K791338
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.1875
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Amdia Medical Products
- Date Received
- July 20, 1979
- Decision Date
- August 10, 1979
- Product Code
- DQD
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DQD | Stethoscope, Electronic | FDA class 2 | Cardiovascular |
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Other Clearances by Amdia Medical Products
| K Number | Device Name | ||
|---|---|---|---|
| K791333 | BOWLES STETHOSCOPE | Aug 10, 1979 | Substantially Equivalent |
| K791335 | NURSESCOPE | Aug 10, 1979 | Substantially Equivalent |
| K791334 | MULTISCOPE | Aug 10, 1979 | Substantially Equivalent |
| K791337 | TAYLOR NEUROLOGICAL HAMMER | Aug 3, 1979 | Substantially Equivalent |
| K791336 | BUCKS NEUROLOGICAL HAMMER | Aug 3, 1979 | Substantially Equivalent |