DISSECTOR

Laparoscope, General & Plastic Surgery

AUTOMATED MEDICAL PRODUCTS CORP.

The following data is part of a premarket notification filed by Automated Medical Products Corp. with the FDA for Dissector.

Pre-market Notification Details

• Device ID: K940199
• 510k Number: K940199
• Device Name: DISSECTOR
• Classification: Laparoscope, General & Plastic Surgery
• Applicant: AUTOMATED MEDICAL PRODUCTS CORP. 646 E. APPLE TREE DR. Sandy, UT 84070
• Contact: Drew D Weaver
• Correspondent: Drew D Weaver; AUTOMATED MEDICAL PRODUCTS CORP. 646 E. APPLE TREE DR. Sandy, UT 84070
• Product Code: GCJ
• CFR Regulation Number: 876.1500 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1994-01-13
• Decision Date: 1994-03-30