Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T)
K260933 is the FDA 510(k) clearance record for Safety Sterile Hypodermic Needles (NR-S1816R, NR-S1916R, NR-S1925R, NR-S1938R, NR-S2016R, NR-S2025R, NR-S2038R, NR-S2051R, NR-S2116R, NR-S2125R, NR-S2138R, NR-S2151R, NR-S2216R, NR-S2225R, NR-S2238R, NR-S2251R, NR-S2316R, NR-S2325R, NR-S2338R, NR-S2351R, NR-S2516R, NR-S2525R, NR-S2538R, NR-S2551R, NR-S2516T, NR-S2525T, NR-S2538T, NR-S2551T), a class II device, cleared for Hangzhou Qiantang Longyue Biotechnology Co., Ltd. on under FDA product code FMI (Needle, Hypodermic, Single Lumen). FDA records list 6 510(k) clearances for Hangzhou Qiantang Longyue Biotechnology Co., Ltd., from to . As of , FDA records show no recalls naming K260933.
Clearance record
- Decision date
- Received
- (140 days to decision)
- Product code
- FMI Needle, Hypodermic, Single Lumen
- Regulation
- 21 CFR 880.5570
- Device class
- Class II
- Review panel
- General Hospital
- Applicant
- Hangzhou Qiantang Longyue Biotechnology Co., Ltd. Rm. 104,201,301,302, Bldg. 12, Block 1,# 619 Wangmei Rd.,, Hangzhou, 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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