MULTIWASH

Station, Pipetting And Diluting, For Clinical Use

FLOW LABORATORIES, INC.

The following data is part of a premarket notification filed by Flow Laboratories, Inc. with the FDA for Multiwash.

Pre-market Notification Details

• Device ID: K813426
• 510k Number: K813426
• Device Name: MULTIWASH
• Classification: Station, Pipetting And Diluting, For Clinical Use
• Applicant: FLOW LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: JQW
• CFR Regulation Number: 862.2750 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1981-12-07
• Decision Date: 1981-12-22