ClearanceBrief
Company ยท US

Advanced Uroscience, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2001. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FBKEndoscopic Injection Needle, Gastroenterology-Urology3
GDWStaple, Implantable1
PAGMesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 3, 2001K001807TISSUE MARKER
Advanced Uroscience, Inc.
GDW
Nov 16, 2000K002573ADVANCED UROSCIENCE INNERSHEATH
Advanced Uroscience, Inc.
FBK
Jul 31, 2000K002323ADVANCED UROSCIENCE INJECTION NEEDLE
Advanced Uroscience, Inc.
FBK
Nov 5, 1999K993459MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
Advanced Uroscience, Inc.
PAG
Oct 26, 1998K982890ADVANCED UROSCIENCE INJECTION NEEDLE
Advanced Uroscience, Inc.
FBK

Latest recalls

DateFirm and productCodeLinked 510(k)
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