HOWMEDICA BITE BLOCK— 510(k) K801911

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K801911 for HOWMEDICA BITE BLOCK, Substantially Equivalent on 1980-08-27. Applicant: Howmedica Corp.. Device class: 1.

Clearance details

Applicant: Howmedica Corp.
Product code: Code EGD
Device class: Class 1
Regulation: 21 CFR 872.6890
Advisory panel: Dental
Date received: 1980-08-11
Decision date: 1980-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code EGD

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