STETH-SHIELD ACCESSORY TO A STETHOSCOPE— 510(k) K882324

Name: FDA 510(k) clearance K882324
Creator: U.S. Food and Drug Administration
Published: 1988-07-18

Substantially Equivalent

Steth-Shield, Inc.

FDA 510(k) clearance K882324 for STETH-SHIELD ACCESSORY TO A STETHOSCOPE, Substantially Equivalent on 1988-07-18. Applicant: Steth-Shield, Inc.. Device class: 1.

Clearance details

Applicant: Steth-Shield, Inc.
Product code: Code LDE
Device class: Class 1
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 1988-06-06
Decision date: 1988-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

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