INJECTOR

Folders And Injectors, Intraocular Lens (iol)

ANTON MEYER & CO. LTD.

The following data is part of a premarket notification filed by Anton Meyer & Co. Ltd. with the FDA for Injector.

Pre-market Notification Details

• Device ID: K023737
• 510k Number: K023737
• Device Name: INJECTOR
• Classification: Folders And Injectors, Intraocular Lens (iol)
• Applicant: ANTON MEYER & CO. LTD. HELMSTRASSE 1 Nidau, CH Ch-2560
• Contact: Thomas Meyer
• Correspondent: Thomas Meyer; ANTON MEYER & CO. LTD. HELMSTRASSE 1 Nidau, CH Ch-2560
• Product Code: MSS
• CFR Regulation Number: 886.4300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2002-11-07
• Decision Date: 2003-07-14
• Summary: summary