FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Hemospray Endoscopic Hemostat (HEMO-[X])

K Number: K253302 · Decision Jun 2, 2026
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
125
Review Days
246

Basic Information

Device Name
Hemospray Endoscopic Hemostat (HEMO-[X])
K Number
K253302
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4456
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Wilson-Cook Medical, Inc.
Date Received
September 29, 2025
Decision Date
June 2, 2026
Product Code
QAU
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QAU Hemostatic Device For Endoscopic Gastrointestinal Use

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (QAU), ordered by most recent decision date.

View all

Other Clearances by Wilson-Cook Medical, Inc.

K Number Device Name
K243568 Teslatome Bipolar Sphincterotome; Tesla BiCord Active Cord
K213356 Entuit PEG, Entuit PEGJ
K212323 Instinct Plus Endoscopic Clipping Device
K201322 Entuit Nasal Jejunal Feeding Tube
K200972 Hemospray Endoscopic Hemostat
K200247 Fusion Quattro Extraction Balloon
K192339 TeslaTome Bipolar Sphincterotome, Tesla Bipolar Active Cord
K193344 Tri-Ex Extraction Balloon with Multiple Sizing
K192908 Fusion Cytology Brush, CytoMax II Double Lumen Cytology Brushes
K191048 AcuSnare Polypectomy Snare - Duckbill
Search all 125 clearances from Wilson-Cook Medical, Inc. →