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)
K240886 is the FDA 510(k) clearance record for 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), a class II device, cleared for Hologic, Inc. on under FDA product code HIG (Insufflator, Hysteroscopic). FDA records list 189 510(k) clearances for Hologic, Inc., from to . As of , FDA records show no recalls naming K240886.
Clearance record
- Decision date
- Received
- (115 days to decision)
- Product code
- HIG Insufflator, Hysteroscopic
- Regulation
- 21 CFR 884.1700
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Hologic, Inc. 250 Campus Dr., Malborough MA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HIG
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 1 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
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