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510(k) K924095

TIMEOSCOPE AND FLEXISCOPE by Stethoscopes of America, Inc. — Product Code LDE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 1992
Date Received
August 13, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stethoscope, Manual
Device Class
Class I
Regulation Number
870.1875
Review Panel
CV
Submission Type

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  • K895545 — V*S*R(TM) SCOPE (November 15, 1989)