510(k) K897195

A-COMPANY ELECTROTHERMAL DEBONDING DEVICE (ETD) by A Company, Inc. — Product Code EKS

K897195 is an FDA 510(k) premarket notification submitted by A Company, Inc. for the device "A-COMPANY ELECTROTHERMAL DEBONDING DEVICE (ETD)". The FDA issued a decision of Substantially Equivalent on May 31, 1990. The device falls under product code EKS (File, Pulp Canal, Endodontic), a Class I device regulated under 21 CFR 872.4565. A Company, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 31, 1990
Date Received
December 29, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
File, Pulp Canal, Endodontic
Device Class
Class I
Regulation Number
872.4565
Review Panel
DE
Submission Type