K202681Substantially Equivalent
Promisemed Covered Safety Pen Needle
Promisemed Hangzhou Meditech Co.,Ltd., Hangzhou City, CN / Special, Substantially Equivalent
K202681 is the FDA 510(k) clearance record for Promisemed Covered Safety Pen Needle, a class II device, cleared for Promisemed Hangzhou Meditech Co., Ltd. on under FDA product code FMI (Needle, Hypodermic, Single Lumen). FDA records list 35 510(k) clearances for Promisemed Hangzhou Meditech Co., Ltd., from to . As of , FDA records show no recalls naming K202681.
Clearance record
- Decision date
- Received
- (107 days to decision)
- Product code
- FMI Needle, Hypodermic, Single Lumen
- Regulation
- 21 CFR 880.5570
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Promisemed Hangzhou Meditech Co., Ltd. # 1388 Cangxing St., Hangzhou City, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code FMI
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 0 |
| January 2026 | 1 |
| February 2026 | 0 |
| March 2026 | 3 |
| April 2026 | 1 |
| May 2026 | 0 |
| June 2026 | 1 |
| July 2026 | 2 |
| August 2026 | 3 |
| September 2026 | 1 |
| October 2026 | 0 |
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