BILSOM PROPP— 510(k) K791608

Name: FDA 510(k) clearance K791608
Creator: U.S. Food and Drug Administration
Published: 1979-10-10

Substantially Equivalent

Bilson International, Inc.

FDA 510(k) clearance K791608 for BILSOM PROPP, Substantially Equivalent on 1979-10-10. Applicant: Bilson International, Inc.. Device class: Unclassified.

Clearance details

Applicant: Bilson International, Inc.
Product code: Code EWD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1979-08-13
Decision date: 1979-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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