BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES— 510(k) K911606

Name: FDA 510(k) clearance K911606
Creator: U.S. Food and Drug Administration
Published: 1991-07-09

Unknown

Baxter Healthcare Corp

FDA 510(k) clearance K911606 for BAXTER PREOPERATIVE SKIN PREP TRAY W/FOAM SPONGES, Unknown on 1991-07-09. Applicant: Baxter Healthcare Corp. Device class: 1.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code KDD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1991-04-10
Decision date: 1991-07-09
Decision: Unknown
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

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