CYPRESS MEDICAL PRODUCTS STETHOSCOPE— 510(k) K945082

Substantially Equivalent

Cypress Medical Products, Ltd.

FDA 510(k) clearance K945082 for CYPRESS MEDICAL PRODUCTS STETHOSCOPE, Substantially Equivalent on 1994-12-08. Applicant: Cypress Medical Products, Ltd..

Clearance details

Applicant: Cypress Medical Products, Ltd.
Product code: Code LDE
Advisory panel: Cardiovascular
Date received: 1994-10-17
Decision date: 1994-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mc Henry, IL, US

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