3M LITTMANN GRAPHIC DISPLAY SYSTEM— 510(k) K920009

Name: FDA 510(k) clearance K920009
Creator: U.S. Food and Drug Administration
Published: 1992-10-21

Substantially Equivalent

3M Health Care, Ltd.

FDA 510(k) clearance K920009 for 3M LITTMANN GRAPHIC DISPLAY SYSTEM, Substantially Equivalent on 1992-10-21. Applicant: 3M Health Care, Ltd.. Device class: 2.

Clearance details

Applicant: 3M Health Care, Ltd.
Product code: Code DQD
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1992-01-02
Decision date: 1992-10-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQD

view all

K261494 — Smart Wireless Stethoscope (4 models)2026-07-31
K261694 — CORE 300 Digital Stethoscope2026-07-23
K252915 — AiSteth®2026-05-22
K252089 — Tyto Stethoscope (G3)2026-03-12
K252076 — Kneevoice Cartilage Evaluation System (750-3600-001)2026-02-06

More clearances from 3M Health Care, Ltd.

view all

K953904 — SARNS 9000 UNIVERSAL ROLLER PUMP1996-04-19
K926364 — ATTEST BRAND RAPID READOUT BIOLOGICAL IND. #129X1995-03-31
K941534 — MODULAR VS-22 CEMENTED FEMORAL HIP SYSTEM1995-03-06
K941748 — STERI-VAC GAS STERILIZER MODEL 8XL1994-12-02
K930681 — 3M PREVENTION FABRIC SURGICAL GOWN #78XX1994-02-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.