The following data is part of a premarket notification filed by Well Lead Medical Instruments with the FDA for Well Lead Silicone And Latex Foley Catheters.
Device ID | K082815 |
510k Number | K082815 |
Device Name: | WELL LEAD SILICONE AND LATEX FOLEY CATHETERS |
Classification | Catheter, Retention Type, Balloon |
Applicant | WELL LEAD MEDICAL INSTRUMENTS A4-1# JINHU INDUSTRIAL ESTATE, HUALONG, PAN YU Guangdong, CN 511434 |
Contact | Han Guang Yuan |
Correspondent | Daniel W Lehtonen INTERTEK TESTING SERVICES 2307 EAST AURORA ROAD UNIT B7 Twinsburg, OH 44087 |
Product Code | EZL |
CFR Regulation Number | 876.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2008-09-25 |
Decision Date | 2008-10-08 |
Summary: | summary |