510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K131531Substantially Equivalent

Tiankang Disposable Syringes with Re-Use Prevention Feature with or without Needle

Anhui Tiankang Medical Products Co., Ltd., Tianchang City, Anhui Province, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K131531 is the FDA 510(k) clearance record for TIANKANG DISPOSABLE SYRINGES WITH RE-USE PREVENTION FEATURE WITH OR WITHOUT NEEDLE, a class II device, cleared for Anhui Tiankang Medical Products Co., Ltd. on under FDA product code MEG (Syringe, Antistick). FDA records list one 510(k) clearance for Anhui Tiankang Medical Products Co., Ltd. As of , FDA records show no recalls naming K131531.

Clearance record

Decision date
Received
(349 days to decision)
Product code
MEG Syringe, Antistick
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Anhui Tiankang Medical Products Co., Ltd. # 20 S. Renhe Rd., Tianchang City, Anhui Province, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MEG

Trailing 12 months
2 clearances under product code MEG in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MEG, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260