DISPOSINEEDLE SHARPS DISPOSAL UNIT— 510(k) K897095

Name: FDA 510(k) clearance K897095
Creator: U.S. Food and Drug Administration
Published: 1990-01-17

Substantially Equivalent

Specialites Septodont

FDA 510(k) clearance K897095 for DISPOSINEEDLE SHARPS DISPOSAL UNIT, Substantially Equivalent on 1990-01-17. Applicant: Specialites Septodont. Device class: 2.

Clearance details

Applicant: Specialites Septodont
Product code: Code MMK
Device class: Class 2
Regulation: 21 CFR 880.5570
Advisory panel: General Hospital
Date received: 1989-12-21
Decision date: 1990-01-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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