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Littman Tunable Stethoscope 2136
FDA 510(k)Class I (US FDA 510(k))
510(k) K821909
by 3m Company
Identifiers
- 510(k) Number
- K821909 FDA 510(k)
- FDA Product Code
- LDE FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 870.1875 FDA 510(k)
- Regulation Number
- 870.1875 FDA 510(k)
- Advisory Committee
- Cardiovascular FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Littman Tunable Stethoscope 2136 by 3m Company — Class I — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K821909 | Class I | Active |
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Manufacturer
- Manufacturer
- 3m Company
Sources (1)
- FDA 510(k) K821909 24 fields · synced Jun 19, 2026