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FDA 510(k), K042936, SOLUTION ADMINISTRATION WITH LUER ACCESS INJECTION SITE
FDA 510(k), K042936, SOLUTION ADMINISTRATION WITH LUER ACCESS INJECTION SITE
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510(K) Number: K042936
Device Name: SOLUTION ADMINISTRATION WITH LUER ACCESS INJECTION SITE
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 10/25/2004
Decision Date: 11/26/2004
Regulation Medical Specialty: General Hospital
Device Name: SOLUTION ADMINISTRATION WITH LUER ACCESS INJECTION SITE
Manufacturer: BAXTER HEALTHCARE CORP.
Device Classification Name: Set, Administration, Intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 10/25/2004
Decision Date: 11/26/2004
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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