510(k) K862866

MODEL 10-C W/LP-10A/U & OS-10A/U FOR ORAL/ENT USE by Directed Energy, Inc. — Product Code EWG

K862866 is an FDA 510(k) premarket notification submitted by Directed Energy, Inc. for the device "MODEL 10-C W/LP-10A/U & OS-10A/U FOR ORAL/ENT USE". The FDA issued a decision of Substantially Equivalent on January 9, 1987. The device falls under product code EWG (Laser, Ent Microsurgical Carbon-Dioxide), a Class II device regulated under 21 CFR 874.4500. Directed Energy, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 9, 1987
Date Received
July 29, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Laser, Ent Microsurgical Carbon-Dioxide
Device Class
Class II
Regulation Number
874.4500
Review Panel
EN
Submission Type