PLEASURE PLUS

Condom

MEDIMIX PRODUCTS, INC.

The following data is part of a premarket notification filed by Medimix Products, Inc. with the FDA for Pleasure Plus.

Pre-market Notification Details

• Device ID: K902772
• 510k Number: K902772
• Device Name: PLEASURE PLUS
• Classification: Condom
• Applicant: MEDIMIX PRODUCTS, INC. MCKENNA, CONNER & CUNEO 1575 EYE STREET, N.W. Washington, DC 20005
• Contact: Martin J Hahn
• Correspondent: Martin J Hahn; MEDIMIX PRODUCTS, INC. MCKENNA, CONNER & CUNEO 1575 EYE STREET, N.W. Washington, DC 20005
• Product Code: HIS
• CFR Regulation Number: 884.5300 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1990-06-22
• Decision Date: 1991-08-14

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00850002174786	K902772	000
00022600999317	K902772	000