MANUAL STETOSCOPE— 510(k) K940578

Substantially Equivalent

Bhs Intl., Inc.

FDA 510(k) clearance K940578 for MANUAL STETOSCOPE, Substantially Equivalent on 1994-04-26. Applicant: Bhs Intl., Inc.. Device class: 1.

Clearance details

Applicant: Bhs Intl., Inc.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1994-02-08
Decision date: 1994-04-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Crofton, MD, US

Download summary PDF View on FDA.gov ↗

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