510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K983367Substantially Equivalent

Qlicksmart

Handren Assoc., Leesburg FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K983367 is the FDA 510(k) clearance record for QLICKSMART, a class II device, cleared for Handren Assoc. on under FDA product code MMK (Container, Sharps). FDA records list one 510(k) clearance for Handren Assoc. As of , FDA records show no recalls naming K983367.

Clearance record

Decision date
Received
(43 days to decision)
Product code
MMK Container, Sharps
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Handren Assoc. 5818 Pr. Caroline Pl., Leesburg FL
510(k) summary
Statement
Third party review
No

Clearances, product code MMK

Trailing 12 months
3 clearances under product code MMK 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 MMK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20261
September 20260
October 20260