KEVOR-CURETTE

Sampler, Endocervical

EURO-MED INTL.

The following data is part of a premarket notification filed by Euro-med Intl. with the FDA for Kevor-curette.

Pre-market Notification Details

• Device ID: K882404
• 510k Number: K882404
• Device Name: KEVOR-CURETTE
• Classification: Sampler, Endocervical
• Applicant: EURO-MED INTL. P.O. BOX 1367 Alameda, CA 94501
• Contact: Karl Hall
• Correspondent: Karl Hall; EURO-MED INTL. P.O. BOX 1367 Alameda, CA 94501
• Product Code: PCF
• CFR Regulation Number: 884.1050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1988-06-10
• Decision Date: 1988-07-08

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20888937003257	K882404	000