Deflecting Ureteral Access Sheath
K030642 is the FDA 510(k) clearance record for DEFLECTING URETERAL ACCESS SHEATH, a class II device, cleared for Applied Medical Resources Corp. on under FDA product code FED (Endoscopic Access Overtube, Gastroenterology-Urology). FDA's definition for product code FED reads: "To facilitate passage and aid advancement of endoscopes into the body, especially in cases of repeated intubation". FDA records list 115 510(k) clearances for Applied Medical Resources Corp., from to . As of , FDA records show no recalls naming K030642.
Clearance record
- Decision date
- Received
- (84 days to decision)
- Product code
- FED Endoscopic Access Overtube, Gastroenterology-Urology
- Regulation
- 21 CFR 876.1500
- Device class
- Class II
- Review panel
- Gastroenterology, Urology
- Applicant
- Applied Medical Resources Corp. 22872 Avenida Empresa, Rancho Santa CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code FED
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 3 |
| October 2026 | 0 |
| November 2026 | 0 |
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