Product code LDE— Cardiovascular
STETHOSCOPE
- Classification name
- Stethoscope, Manual
- Device class
- Class 1
- Regulation
- 21 CFR 870.1875
- Advisory panel
- Cardiovascular
- Total cleared
- 28
- First cleared
- Most recent
Market context for product code LDE
FDA has cleared devices under product code LDE between 1978 and 1994, filed by 25 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1994
- 1992
- 1991
- 1989
- 1988
- 1987
- 1986
- 1985
- 1983
- 1982
- 1981
- 1980
- 1978
Top applicants under product code LDE
Recent clearances under product code LDE
- K945082 — CYPRESS MEDICAL PRODUCTS STETHOSCOPE
- K944337 — VARIOUS STETHOSCOPES
- K940578 — MANUAL STETOSCOPE
- K935944 — PROSCOPES AND ADSCOPES
- K923327 — STETHOSCOPE COVER
- K924095 — TIMEOSCOPE AND FLEXISCOPE
- K914100 — STETHOSCOPE
- K912128 — MAXI-SCOPE OR ULTRA-SCOPE
- K905487 — VARIOUS TYPES OF STETHOSCOPES
- K904547 — STETHOSCOPE
- K895545 — V*S*R(TM) SCOPE
- K890126 — KAMED STETHOSCOPE
- K882324 — STETH-SHIELD ACCESSORY TO A STETHOSCOPE
- K871369 — VARIOUS TYPES OF: KEELER MAGNATONE 2 STETHOSCOPES:
- K860473 — DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE
- K854771 — SALTZMAN STETHOSCOPE HEAD
- K842203 — LITTMAN TYPE SH-6010, NURSE TYPE
- K843324 — SPRAGUE RAPPAPORT/SH-6008 DISPOS. STETH
- K830796 — THE BLOOM STETHOSCOPE
- K821909 — LITTMAN TUNABLE STETHOSCOPE 2136
- K813510 — CARDIOSONIC ACOUSTIC AMPLIFIER
- K812676 — AMPLITONE-3
- K801811 — PALPATION ENHANCER
- K801183 — CONPHAR DUAL HEAD STETHOSCOPE
- K801184 — CONPHAR SPRAGUE RAPPAPORT STETHOSCOPE
- K801185 — CONPHAR BOWLS STETHOSCOPE
- K801215 — ABCO PEDIATRIC STETHOSCOPE
- K780023 — BLACK BAG, ELECTRONIC
Data sourced from openFDA. This site is unofficial and independent of the FDA.