The following data is part of a premarket notification filed by Annex Medical, Inc. with the FDA for Dislodger, Stone, Basket, Ureteral, Metal.
Device ID | K924027 |
510k Number | K924027 |
Device Name: | DISLODGER, STONE, BASKET, URETERAL, METAL |
Classification | Dislodger, Stone, Basket, Ureteral, Metal |
Applicant | ANNEX MEDICAL, INC. 7887 FULLER RD. #109 Eden Prairie, MN 55344 |
Contact | Daniel L Dostal |
Correspondent | Daniel L Dostal ANNEX MEDICAL, INC. 7887 FULLER RD. #109 Eden Prairie, MN 55344 |
Product Code | FFL |
CFR Regulation Number | 876.4680 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-08-11 |
Decision Date | 1992-10-20 |