510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K860473Substantially Equivalent

Differential Stethoscope W/dual Heads; Stereoscope

Schering Corp., Kenilworth NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860473 is the FDA 510(k) clearance record for DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE, a class I device, cleared for Schering Corp. on under FDA product code LDE (Stethoscope, Manual). FDA records list one 510(k) clearance for Schering Corp. As of , FDA records show no recalls naming K860473.

Clearance record

Decision date
Received
(189 days to decision)
Product code
LDE Stethoscope, Manual
Regulation
21 CFR 870.1875
Device class
Class I
Review panel
Cardiovascular
Applicant
Schering Corp. 2000 Galloping Hill Rd., Kenilworth NJ
Third party review
No

Clearances, product code LDE

Trailing 12 months

FDA records hold no clearances under product code LDE in the trailing twelve months.

FDA records show no clearances under product code LDE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDE, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260