510(k) K853902

ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGY by Endo Lase, Inc. — Product Code EWG

K853902 is an FDA 510(k) premarket notification submitted by Endo Lase, Inc. for the device "ENDO-LASE CD40 FOR OTORHINOLARYNGOLOGY". The FDA issued a decision of Substantially Equivalent on January 9, 1986. The device falls under product code EWG (Laser, Ent Microsurgical Carbon-Dioxide), a Class II device regulated under 21 CFR 874.4500. Endo Lase, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 9, 1986
Date Received
September 20, 1985
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