SURESCAN

Powered Laser Surgical Instrument

CLINICON CORP.

The following data is part of a premarket notification filed by Clinicon Corp. with the FDA for Surescan.

Pre-market Notification Details

• Device ID: K962242
• 510k Number: K962242
• Device Name: SURESCAN
• Classification: Powered Laser Surgical Instrument
• Applicant: CLINICON CORP. 2182 EL CAMINO REAL SUITE 209 Oceanside, CA 92054
• Contact: Alan Bunting
• Correspondent: Alan Bunting; CLINICON CORP. 2182 EL CAMINO REAL SUITE 209 Oceanside, CA 92054
• Product Code: GEX
• CFR Regulation Number: 878.4810 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1996-06-11
• Decision Date: 1996-09-03
• Summary: summary