I.V. ADMINISTRATION SET

Set, Administration, Intravascular

RESEARCH INDUSTRIES CORP.

The following data is part of a premarket notification filed by Research Industries Corp. with the FDA for I.v. Administration Set.

Pre-market Notification Details

• Device ID: K832542
• 510k Number: K832542
• Device Name: I.V. ADMINISTRATION SET
• Classification: Set, Administration, Intravascular
• Applicant: RESEARCH INDUSTRIES CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: FPA
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-07-29
• Decision Date: 1983-10-31