JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE— 510(k) K800623

Name: FDA 510(k) clearance K800623
Creator: U.S. Food and Drug Administration
Published: 1980-04-24

Substantially Equivalent

Pilling Co.

FDA 510(k) clearance K800623 for JACKSON ESOPHAGEAL BOUGIE, X-RAY OPAQUE, Substantially Equivalent on 1980-04-24. Applicant: Pilling Co.. Device class: 1.

Clearance details

Applicant: Pilling Co.
Product code: Code KCD
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Date received: 1980-03-19
Decision date: 1980-04-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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