'EXMOOR' DAS GUPTA LARYNGEAL KEEL— 510(k) K864936

Name: FDA 510(k) clearance K864936
Creator: U.S. Food and Drug Administration
Published: 1987-04-27

Substantially Equivalent

Exmoor Plastics , Ltd.

FDA 510(k) clearance K864936 for 'EXMOOR' DAS GUPTA LARYNGEAL KEEL, Substantially Equivalent on 1987-04-27. Applicant: Exmoor Plastics , Ltd.. Device class: 2.

Clearance details

Applicant: Exmoor Plastics , Ltd.
Product code: Code FWN
Device class: Class 2
Regulation: 21 CFR 874.3620
Advisory panel: Ear, Nose, Throat
Date received: 1986-12-16
Decision date: 1987-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taunton, GB

Download summary PDF View on FDA.gov ↗

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