K210355Substantially Equivalent
Surgical Gown, Model: surgical gown-hp-3
Weihai Dishang Medical Technology Co.,Ltd, Weihai, CN / Traditional, Substantially Equivalent
K210355 is the FDA 510(k) clearance record for Surgical Gown, Model: surgical gown-hp-3, a class II device, cleared for Weihai Dishang Medical Technology Co., Ltd. on under FDA product code FYA (Gown, Surgical). FDA records list 2 510(k) clearances for Weihai Dishang Medical Technology Co., Ltd., from to . As of , FDA records show no recalls naming K210355.
Clearance record
- Decision date
- Received
- (311 days to decision)
- Product code
- FYA Gown, Surgical
- Regulation
- 21 CFR 878.4040
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- Weihai Dishang Medical Technology Co., Ltd. Rm. 406-409, Block C, #213 Torch Rd.,, Weihai, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code FYA
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 1 |
| January 2026 | 0 |
| February 2026 | 2 |
| March 2026 | 0 |
| April 2026 | 2 |
| May 2026 | 1 |
| June 2026 | 1 |
| July 2026 | 1 |
| August 2026 | 2 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
