RETRACTOR

Retractor

AUTOMATED MEDICAL PRODUCTS CORP.

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

Pre-market Notification Details

• Device ID: K942002
• 510k Number: K942002
• Device Name: RETRACTOR
• Classification: Retractor
• Applicant: AUTOMATED MEDICAL PRODUCTS CORP. 2315 BROADWAY, SUITE 410 New York, NY 10024
• Contact: Gregory Diamant
• Correspondent: Gregory Diamant; AUTOMATED MEDICAL PRODUCTS CORP. 2315 BROADWAY, SUITE 410 New York, NY 10024
• Product Code: GAD
• CFR Regulation Number: 878.4800 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1994-04-25
• Decision Date: 1994-05-17