SHILEY CRICOTHYROTOMY TUBE— 510(k) K781639

Substantially Equivalent

Shiley, Inc.

FDA 510(k) clearance K781639 for SHILEY CRICOTHYROTOMY TUBE, Substantially Equivalent on 1978-10-24. Applicant: Shiley, Inc.. Device class: 2.

Clearance details

Applicant: Shiley, Inc.
Product code: Code EQN
Device class: Class 2
Regulation: 21 CFR 874.4760
Advisory panel: Ear, Nose, Throat
Date received: 1978-09-21
Decision date: 1978-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.