FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Asurys Fluid Management System
K Number: K251273
·
Decision Mar 27, 2026
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
55
Applicant Total
231
Review Days
337
Basic Information
- Device Name
- Asurys Fluid Management System
- K Number
- K251273
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.1700
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Boston Scientific Corporation
- Date Received
- April 24, 2025
- Decision Date
- March 27, 2026
- Product Code
- HIG
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HIG | Insufflator, Hysteroscopic | FDA class 2 | Obstetrics/Gynecology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HIG), ordered by most recent decision date.
Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap Multipack (10-pack) (FLT-210); Fluent Pro Fluid Management System Waste Bag Multipack (5-pack) (FLT-205)
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Fluent Fluid Management System
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FDA Class 2
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