FDA Device Intelligence
Home › 3M COMPANY › 3M™ Littmann® Classic III™

3M™ Littmann® Classic III™

3M COMPANY · Model 5870 · UDI-DI 00707387790356

LDE
10
510(k) clearances
29
Adverse events
0
Recalls
181
Facilities

Description

3M™ Littmann® Classic III™ Monitoring Stethoscope, 5870, Rainbow-Finish Chestpiece, black stem and headset, Black Tube

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.