PHARMULATOR

Set, I.v. Fluid Transfer

ACACIA, INC.

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

Pre-market Notification Details

• Device ID: K896990
• 510k Number: K896990
• Device Name: PHARMULATOR
• Classification: Set, I.v. Fluid Transfer
• Applicant: ACACIA, INC. P.O. BOX 1240 Loma Linda, CA 92354
• Contact: Margaret Lumia,pharm
• Correspondent: Margaret Lumia,pharm; ACACIA, INC. P.O. BOX 1240 Loma Linda, CA 92354
• Product Code: LHI
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1989-12-13
• Decision Date: 1990-03-23