LIFECELL RECOVERY CONTAINER— 510(k) K893787

Name: FDA 510(k) clearance K893787
Creator: U.S. Food and Drug Administration
Published: 1989-06-23

Substantially Equivalent

Baxter Healthcare Corp

FDA 510(k) clearance K893787 for LIFECELL RECOVERY CONTAINER, Substantially Equivalent on 1989-06-23. Applicant: Baxter Healthcare Corp. Device class: 1.

Clearance details

Applicant: Baxter Healthcare Corp
Product code: Code KJF
Device class: Class 1
Regulation: 21 CFR 864.2240
Advisory panel: Hematology
Date received: 1989-05-22
Decision date: 1989-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Round Lake, IL, US

Download summary PDF View on FDA.gov ↗

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