LDE · Class I · 21 CFR 870.1875

FDA Product Code LDE: Stethoscope, Manual

Leading manufacturers include Conphar, Inc., 3M Company and Keeler Instruments, Inc..

28
Total
28
Cleared
94d
Avg days
1978
Since

FDA 510(k) Cleared Stethoscope, Manual Devices (Product Code LDE)

28 devices
1–24 of 28
Cleared Dec 08, 1994
CYPRESS MEDICAL PRODUCTS STETHOSCOPE
K945082
Cypress Medical Products, Ltd.
Cardiovascular · 52d
Cleared Mar 03, 1994
PROSCOPES AND ADSCOPES
K935944
American Diagnostic Corp.
Cardiovascular · 80d
Cleared Sep 24, 1987
VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:
K871369
Keeler Instruments, Inc.
Cardiovascular · 170d
Cleared Jul 14, 1982
LITTMAN TUNABLE STETHOSCOPE 2136
K821909
3M Company
Cardiovascular · 16d
Cleared Jun 04, 1980
CONPHAR DUAL HEAD STETHOSCOPE
K801183
Conphar, Inc.
Cardiovascular · 19d
Cleared Jun 04, 1980
CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE
K801184
Conphar, Inc.
Cardiovascular · 19d
Cleared Jun 04, 1980
CONPHAR BOWLS STETHOSCOPE
K801185
Conphar, Inc.
Cardiovascular · 16d
Cleared Jun 04, 1980
ABCO PEDIATRIC STETHOSCOPE
K801215
Abco Dealers, Inc.
Cardiovascular · 15d

About Product Code LDE - Regulatory Context