DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE— 510(k) K860473

Name: FDA 510(k) clearance K860473
Creator: U.S. Food and Drug Administration
Published: 1986-08-14

Substantially Equivalent

Schering Corp.

FDA 510(k) clearance K860473 for DIFFERENTIAL STETHOSCOPE W/DUAL HEADS; STEREOSCOPE, Substantially Equivalent on 1986-08-14. Applicant: Schering Corp.. Device class: 1.

Clearance details

Applicant: Schering Corp.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1986-02-06
Decision date: 1986-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kenilworth, NJ, US

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