MODULAP

Laparoscope, General & Plastic Surgery

ATC TECHNOLOGIES, INC.

The following data is part of a premarket notification filed by Atc Technologies, Inc. with the FDA for Modulap.

Pre-market Notification Details

• Device ID: K983623
• 510k Number: K983623
• Device Name: MODULAP
• Classification: Laparoscope, General & Plastic Surgery
• Applicant: ATC TECHNOLOGIES, INC. 1034 LINCOLN ST. Hollywood, FL 33019
• Contact: Marian Harding Cochran
• Correspondent: Marian Harding Cochran; ATC TECHNOLOGIES, INC. 1034 LINCOLN ST. Hollywood, FL 33019
• Product Code: GCJ
• CFR Regulation Number: 876.1500 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1998-10-15
• Decision Date: 1998-12-18
• Summary: summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
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