The following data is part of a premarket notification filed by Candela Laser Corp. with the FDA for Candela Stone Baskets.
Device ID | K884738 |
510k Number | K884738 |
Device Name: | CANDELA STONE BASKETS |
Classification | Dislodger, Stone, Basket, Ureteral, Metal |
Applicant | CANDELA LASER CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
Contact | George Cho |
Correspondent | George Cho CANDELA LASER CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
Product Code | FFL |
CFR Regulation Number | 876.4680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-14 |
Decision Date | 1989-02-09 |