AUDIOPRAT ENDOSCOPE— 510(k) K903012

Name: FDA 510(k) clearance K903012
Creator: U.S. Food and Drug Administration
Published: 1990-10-09

Substantially Equivalent

S.C.D.P.I. of Florida, Inc.

FDA 510(k) clearance K903012 for AUDIOPRAT ENDOSCOPE, Substantially Equivalent on 1990-10-09. Applicant: S.C.D.P.I. of Florida, Inc.. Device class: 1.

Clearance details

Applicant: S.C.D.P.I. of Florida, Inc.
Product code: Code EHB
Device class: Class 1
Regulation: 21 CFR 872.1840
Advisory panel: Dental
Date received: 1990-07-11
Decision date: 1990-10-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ormond Beach, FL, US

Download summary PDF View on FDA.gov ↗

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