Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube, Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube with ENFit Connection, Entuit LP Patient Care Kit, Entuit LP Patient Care Kit with ENFit Connection, PromaX Low Profile Gastrostomy Feeding Tube, PromaX LP Patient Care Kit with ENFit
K180708 is the FDA 510(k) clearance record for Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube, Entuit LP Gastrostomy BR Low Profile Balloon Retention Feeding Tube with ENFit Connection, Entuit LP Patient Care Kit, Entuit LP Patient Care Kit with ENFit Connection, PromaX Low Profile Gastrostomy Feeding Tube, PromaX LP Patient Care Kit with ENFit, a class II device, cleared for Xeridiem Medical Devices, A Spectrum Plastics Group Company on under FDA product code PIF (Gastrointestinal Tubes With Enteral Specific Connectors). FDA's definition for product code PIF reads: "To facilitate enteral specific connections". FDA records list 2 510(k) clearances for Xeridiem Medical Devices, A Spectrum Plastics Group Company, from to . As of , FDA records show no recalls naming K180708.
Clearance record
- Decision date
- Received
- (213 days to decision)
- Product code
- PIF Gastrointestinal Tubes With Enteral Specific Connectors
- Regulation
- 21 CFR 876.5980
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Applicant
- Xeridiem Medical Devices, A Spectrum Plastics Group Company 4700 S. Overland Dr., Tucson AZ
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code PIF
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 | 0 |
| August 2026 | 1 |
| September 2026 | 1 |
| October 2026 | 0 |
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