The following data is part of a premarket notification filed by Applied Medical Resources Corp. with the FDA for Gelport Single Incision Access System.
Device ID | K090275 |
510k Number | K090275 |
Device Name: | GELPORT SINGLE INCISION ACCESS SYSTEM |
Classification | Laparoscope, General & Plastic Surgery |
Applicant | APPLIED MEDICAL RESOURCES CORP. 22872 Avenida Empresa Rancho Santa Margarita, CA 92688 |
Contact | Frans Vandebbroek |
Correspondent | Morten S Christensen UNDERWRITERS LABORATORIES, INC. 455 E. TRIMBLE ROAD San Jose, CA 95131 -1230 |
Product Code | GCJ |
CFR Regulation Number | 876.1500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2009-02-04 |
Decision Date | 2009-02-18 |
Summary: | summary |