I.V. TRANSFER NEEDLE

Set, I.v. Fluid Transfer

BAXA CORP., SUB. OF COOK GROUP, INC.

The following data is part of a premarket notification filed by Baxa Corp., Sub. Of Cook Group, Inc. with the FDA for I.v. Transfer Needle.

Pre-market Notification Details

• Device ID: K832312
• 510k Number: K832312
• Device Name: I.V. TRANSFER NEEDLE
• Classification: Set, I.v. Fluid Transfer
• Applicant: BAXA CORP., SUB. OF COOK GROUP, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: LHI
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-07-14
• Decision Date: 1983-09-12