DENTAL ANESTHESIA APPARATUS— 510(k) K850425

Name: FDA 510(k) clearance K850425
Creator: U.S. Food and Drug Administration
Published: 1986-10-09

Substantially Equivalent for Some Indications

Pain Prevention, Inc.

FDA 510(k) clearance K850425 for DENTAL ANESTHESIA APPARATUS, Substantially Equivalent for Some Indications on 1986-10-09. Applicant: Pain Prevention, Inc.. Device class: 2.

Clearance details

Applicant: Pain Prevention, Inc.
Product code: Code KZM
Device class: Class 2
Regulation: 21 CFR 890.1375
Advisory panel: Physical Medicine
Date received: 1985-02-04
Decision date: 1986-10-09
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Chicago, IL, 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.