510(k) K822261

LARYNGEAL MIRRORS by Kelleher Corp. — Product Code KAI

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 30, 1982
Date Received
July 29, 1982
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mirror, Ent
Device Class
Class I
Regulation Number
874.4420
Review Panel
EN
Submission Type