510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252899Substantially Equivalent

Female Culture Device; Male Culture Device; Transfer Device; Access Device

Zhejiang Kindly Medical Device Co., Ltd., Wenzhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K252899 is the FDA 510(k) clearance record for Female Culture Device; Male Culture Device; Transfer Device; Access Device, a class II device, cleared for Zhejiang Kindly Medical Device Co., Ltd. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 2 510(k) clearances for Zhejiang Kindly Medical Device Co., Ltd., from to . As of , FDA records show no recalls naming K252899.

Clearance record

Decision date
Received
(264 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Zhejiang Kindly Medical Device Co., Ltd. No 758, 5th Binhai Rd., Binhai Industrial Park, Longwan, Wenzhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260