K221178Substantially Equivalent
Disposable Insulin Pen Needle
Ningbo Medsun Medical Co., Ltd., Ningbo, CN / Traditional, Substantially Equivalent
K221178 is the FDA 510(k) clearance record for Disposable Insulin Pen Needle, a class II device, cleared for Ningbo Medsun Medical Co., Ltd. on under FDA product code FMI (Needle, Hypodermic, Single Lumen). FDA records list 7 510(k) clearances for Ningbo Medsun Medical Co., Ltd., from to . As of , FDA records show no recalls naming K221178.
Clearance record
- Decision date
- Received
- (206 days to decision)
- Product code
- FMI Needle, Hypodermic, Single Lumen
- Regulation
- 21 CFR 880.5570
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Ningbo Medsun Medical Co., Ltd. #55 Jinxi Rd., Zhenhai, Ningbo, 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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