KAMED STETHOSCOPE— 510(k) K890126

Substantially Equivalent

D.R.G.

FDA 510(k) clearance K890126 for KAMED STETHOSCOPE, Substantially Equivalent on 1989-04-21. Applicant: D.R.G.. Device class: 1.

Clearance details

Applicant: D.R.G.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1989-01-12
Decision date: 1989-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mountainside, NJ, US

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Recent devices under product code LDE

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K935944 — PROSCOPES AND ADSCOPES1994-03-03
K923327 — STETHOSCOPE COVER1992-11-03

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