ROBOCAP

Station, Pipetting And Diluting, For Clinical Use

PHARMACIA, INC.

The following data is part of a premarket notification filed by Pharmacia, Inc. with the FDA for Robocap.

Pre-market Notification Details

• Device ID: K952025
• 510k Number: K952025
• Device Name: ROBOCAP
• Classification: Station, Pipetting And Diluting, For Clinical Use
• Applicant: PHARMACIA, INC. 7001 POST RD. Dublin, OH 43017
• Contact: Jean Frydman
• Correspondent: Jean Frydman; PHARMACIA, INC. 7001 POST RD. Dublin, OH 43017
• Product Code: JQW
• CFR Regulation Number: 862.2750 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-05-01
• Decision Date: 1995-07-26