ULTIMAX

Latex Patient Examination Glove

WEMBLEY RUBBER PRODUCTS (M) SDN BHD

The following data is part of a premarket notification filed by Wembley Rubber Products (m) Sdn Bhd with the FDA for Ultimax.

Pre-market Notification Details

• Device ID: K951467
• 510k Number: K951467
• Device Name: ULTIMAX
• Classification: Latex Patient Examination Glove
• Applicant: WEMBLEY RUBBER PRODUCTS (M) SDN BHD 84, JALAN RAJA CHULAN 50200 KUALA LUMPUR Malaysia, MY
• Contact: Ong G Chee
• Correspondent: Ong G Chee; WEMBLEY RUBBER PRODUCTS (M) SDN BHD 84, JALAN RAJA CHULAN 50200 KUALA LUMPUR Malaysia, MY
• Product Code: LYY
• CFR Regulation Number: 880.6250 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-03-30
• Decision Date: 1995-04-28