STETHOSCOPE— 510(k) K904547

Substantially Equivalent

Kimball Industries Co., Ltd.

FDA 510(k) clearance K904547 for STETHOSCOPE, Substantially Equivalent on 1991-03-21. Applicant: Kimball Industries Co., Ltd.. Device class: 1.

Clearance details

Applicant: Kimball Industries Co., Ltd.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1990-10-03
Decision date: 1991-03-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shirley, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LDE

K945082 — CYPRESS MEDICAL PRODUCTS STETHOSCOPE1994-12-08
K944337 — VARIOUS STETHOSCOPES1994-11-30
K940578 — MANUAL STETOSCOPE1994-04-26
K935944 — PROSCOPES AND ADSCOPES1994-03-03
K923327 — STETHOSCOPE COVER1992-11-03

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