The following data is part of a premarket notification filed by Usgi Medical with the FDA for G-prox Endoscopic Grasper, Model 205333.
Device ID | K093018 |
510k Number | K093018 |
Device Name: | G-PROX ENDOSCOPIC GRASPER, MODEL 205333 |
Classification | Suture, Nonabsorbable, Synthetic, Polyethylene |
Applicant | USGI MEDICAL 1140 CALLE CORDILLERA San Clemente, CA 92673 |
Contact | Mary L Mooney |
Correspondent | Mary L Mooney USGI MEDICAL 1140 CALLE CORDILLERA San Clemente, CA 92673 |
Product Code | GAT |
Subsequent Product Code | GDW |
Subsequent Product Code | HET |
CFR Regulation Number | 878.5000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-09-08 |
Decision Date | 2009-10-07 |
Summary: | summary |