LITTMAN TUNABLE STETHOSCOPE 2136— 510(k) K821909
Substantially Equivalent3M Company
FDA 510(k) clearance K821909 for LITTMAN TUNABLE STETHOSCOPE 2136, Substantially Equivalent on 1982-07-14. Applicant: 3M Company. Device class: 1.
Clearance details
- Applicant
- 3M Company
- Product code
- Code LDE
- Device class
- Class 1
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- White City, OR, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.