APPLIC SYSTEM ACTIVATOR, ESPE— 510(k) K770941

Substantially Equivalent

Espe GmbH (Us)

FDA 510(k) clearance K770941 for APPLIC SYSTEM ACTIVATOR, ESPE, Substantially Equivalent on 1977-06-02. Applicant: Espe GmbH (Us). Device class: 1.

Clearance details

Applicant: Espe GmbH (Us)
Product code: Code EID
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1977-05-23
Decision date: 1977-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Espe GmbH (Us)

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K915005 — PHOTAC-BOND APLICAP, MODIFICATION1992-01-14
K913857 — ROCATEC(R) -PLUS1991-12-16
K913965 — ESPE(R) -SIL1991-12-04

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