INTERCEPT

Regulator, Vacuum

VITAL SIGNS, INC.

The following data is part of a premarket notification filed by Vital Signs, Inc. with the FDA for Intercept.

Pre-market Notification Details

• Device ID: K843591
• 510k Number: K843591
• Device Name: INTERCEPT
• Classification: Regulator, Vacuum
• Applicant: VITAL SIGNS, INC. 1 MADISON ST. East Rutherford, NJ 07073
• Contact: Terence D Wall
• Correspondent: Terence D Wall; VITAL SIGNS, INC. 1 MADISON ST. East Rutherford, NJ 07073
• Product Code: KDP
• CFR Regulation Number: 880.6740 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-09-12
• Decision Date: 1984-10-19