ARMI® Endoscopic Video Image Processor (JY-MIP-3000); ARMI® Single-Use Hysteroscope (SH-01A, SH-02A, SH-03A, SH-04A, SH-05A, SH-01B, SH-02B, SH-03B, SH-04B, SH-01C, SH-02C, SH-03C, SH-04C)
K252793 is the FDA 510(k) clearance record for ARMI® Endoscopic Video Image Processor (JY-MIP-3000); ARMI® Single-Use Hysteroscope (SH-01A, SH-02A, SH-03A, SH-04A, SH-05A, SH-01B, SH-02B, SH-03B, SH-04B, SH-01C, SH-02C, SH-03C, SH-04C), a class II device, cleared for Jiangsu Jiyuan Medical Technology Co., Ltd. on under FDA product code HIH (Hysteroscope (And Accessories)). FDA records list 2 510(k) clearances for Jiangsu Jiyuan Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K252793.
Clearance record
- Decision date
- Received
- (111 days to decision)
- Product code
- HIH Hysteroscope (And Accessories)
- Regulation
- 21 CFR 884.1690
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Jiangsu Jiyuan Medical Technology Co., Ltd. # 48 Cecep (Taizhou) Environmental Protection Technology, Taizhou, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HIH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 0 |
| February 2026 | 1 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 1 |
| September 2026 | 3 |
| October 2026 | 0 |
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