Disposable safety lancet (Impress); Disposable safety lancet (Impress Pro); Disposable safety lancet (Lite4); Disposable blood lancet (Elite); Disposable blood lancet (Elite Pro)
K233796 is the FDA 510(k) clearance record for Disposable safety lancet (Impress); Disposable safety lancet (Impress Pro); Disposable safety lancet (Lite4); Disposable blood lancet (Elite); Disposable blood lancet (Elite Pro), a class II device, cleared for SteriLance Medical (Suzhou), Inc. on under FDA product code FMK (Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature). FDA's definition for product code FMK reads: "A disposable blood lancet intended for a single use that is comprised of a single use blade attached to a solid, non-reusable base (including an integral sharps injury prevention feature) that is used to puncture the skin to obtain a drop...". FDA records list 10 510(k) clearances for SteriLance Medical (Suzhou), Inc., from to . As of , FDA records show no recalls naming K233796.
Clearance record
- Decision date
- Received
- (48 days to decision)
- Product code
- FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature
- Regulation
- 21 CFR 878.4850
- Device class
- Class II
- Review panel
- General, Plastic Surgery
- Applicant
- SteriLance Medical (Suzhou), Inc. #168 Putuoshan Rd., Suzhou, CN
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code FMK
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 2 |
| March 2026 | 1 |
| April 2026 | 0 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 1 |
| October 2026 | 0 |
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