510(k) K925789

DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE by Deroyal Industries, Inc. — Product Code BZT

K925789 is an FDA 510(k) premarket notification submitted by Deroyal Industries, Inc. for the device "DEBUSK TEMP. SYST. ESOPHAGEAL STETHOSCOPE". The FDA issued a decision of Substantially Equivalent on July 13, 1993. The device falls under product code BZT (Stethoscope, Esophageal, With Electrical Conductors), a Class II device regulated under 21 CFR 868.1920. Deroyal Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 13, 1993
Date Received
November 16, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stethoscope, Esophageal, With Electrical Conductors
Device Class
Class II
Regulation Number
868.1920
Review Panel
AN
Submission Type