510(k) K864936

'EXMOOR' DAS GUPTA LARYNGEAL KEEL by Exmoor Plastics , Ltd. — Product Code FWN

K864936 is an FDA 510(k) premarket notification submitted by Exmoor Plastics , Ltd. for the device "'EXMOOR' DAS GUPTA LARYNGEAL KEEL". The FDA issued a decision of Substantially Equivalent on April 27, 1987. The device falls under product code FWN (Prosthesis, Larynx (Stents And Keels)), a Class II device regulated under 21 CFR 874.3620. Exmoor Plastics , Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 27, 1987
Date Received
December 16, 1986
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Larynx (Stents And Keels)
Device Class
Class II
Regulation Number
874.3620
Review Panel
EN
Submission Type