FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
LITTMAN TUNABLE STETHOSCOPE 2136
K Number: K821909
·
Decision Jul 14, 1982
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
27
Applicant Total
331
Review Days
16
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Basic Information
- Device Name
- LITTMAN TUNABLE STETHOSCOPE 2136
- K Number
- K821909
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 870.1875
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- 3M Company
- Date Received
- June 28, 1982
- Decision Date
- July 14, 1982
- Product Code
- LDE
- 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 |
|---|---|---|---|
| LDE | Stethoscope, Manual | FDA class 1 | Cardiovascular |
Similar 510(k) Clearances
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TIMEOSCOPE AND FLEXISCOPE
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