SPOROX II STERILIZING & DISINFECTING SOLUTION— 510(k) K990703

Name: FDA 510(k) clearance K990703
Creator: U.S. Food and Drug Administration
Published: 1999-03-30

Substantially Equivalent

Reckitt Benckiser, Inc.

FDA 510(k) clearance K990703 for SPOROX II STERILIZING & DISINFECTING SOLUTION, Substantially Equivalent on 1999-03-30. Applicant: Reckitt Benckiser, Inc.. Device class: 2.

Clearance details

Applicant: Reckitt Benckiser, Inc.
Product code: Code MED
Device class: Class 2
Regulation: 21 CFR 880.6885
Advisory panel: General Hospital
Date received: 1999-03-04
Decision date: 1999-03-30
Decision: Substantially Equivalent
Clearance type: Special
Location: Wayne, NJ, US

Download summary PDF View on FDA.gov ↗

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