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 |