EDENTEC MODEL 4700 SCANNER— 510(k) K884388

Substantially Equivalent

Edentec Corp.

FDA 510(k) clearance K884388 for EDENTEC MODEL 4700 SCANNER, Substantially Equivalent on 1989-01-10. Applicant: Edentec Corp.. Device class: 1.

Clearance details

Applicant: Edentec Corp.
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1988-10-18
Decision date: 1989-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

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