510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213010Substantially Equivalent

FEELject LDV (Low dead volume) syringe

Feeltech Co.,Ltd., Gunsan-Si, KR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213010 is the FDA 510(k) clearance record for FEELject LDV (Low dead volume) syringe, a class II device, cleared for Feeltech Co., Ltd. on under FDA product code QNQ (Low Dead Space Piston Syringe). FDA's definition for product code QNQ reads: "A low dead space syringe is a piston syringe designed to reduce medication waste. The device consists of a calibrated hollow barrel, a moveable plunger, and may include a needle. The device can be used by health care professions or for...". FDA records list 4 510(k) clearances for Feeltech Co., Ltd., from to . As of , FDA records show no recalls naming K213010.

Clearance record

Decision date
Received
(618 days to decision)
Product code
QNQ Low Dead Space Piston Syringe
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Applicant
Feeltech Co., Ltd. 3, 4 Floor, Standard Factory, 2-Dong, 15 Jayumuyeok2-Gil, Gunsan-Si, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QNQ

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