UNICIDE

Solution, Cold Sterilizing

NORTH PACIFIC DENTAL, INC.

The following data is part of a premarket notification filed by North Pacific Dental, Inc. with the FDA for Unicide.

Pre-market Notification Details

• Device ID: K830106
• 510k Number: K830106
• Device Name: UNICIDE
• Classification: Solution, Cold Sterilizing
• Applicant: NORTH PACIFIC DENTAL, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: LFE
• CFR Regulation Number: 880.6885 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-01-11
• Decision Date: 1983-03-07