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Morimatsu, M., Mekhdjian, A

The commenter also noted that 1 month after C1747 was established based on the approval of the STERIS Uretero1 TM device pass-through application, FDA granted the LithoVue TM Elite System 510(k) clearance, on February 2, 2023

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Peeker R, Aldenborg F and Fall M: The treatment of interstitial cystitis with supratrigonal cystectomy and ileocystoplasty: Difference in outcome between classic and nonulcer disease

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