Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K200839Substantially Equivalent

APAS Independence with IC Chromogenic MRSA BD Analysis Module; APAS Independence with IC Chromogenic MRSA TFS/S Analysis Module

Clever Culture Systems Limited, Bach, CH / Traditional, Substantially Equivalent

K200839 is the FDA 510(k) clearance record for APAS Independence with IC Chromogenic MRSA BD Analysis Module; APAS Independence with IC Chromogenic MRSA TFS/S Analysis Module, a class II device, cleared for Clever Culture Systems on under FDA product code QQY (Culture Plate Imaging System For Qualitative Assessment Of Resistant Organisms). FDA's definition for product code QQY reads: "Culture plate imaging system for qualitative assessment of resistant organisms is an automated system to assess the presence or absence of colony growth on solid chromogenic culture media". FDA records list 3 510(k) clearances for Clever Culture Systems, from to . As of , FDA records show no recalls naming K200839.

Clearance record

Decision date
Received
(576 days to decision)
Product code
QQY Culture Plate Imaging System For Qualitative Assessment Of Resistant Organisms
Regulation
21 CFR 866.2190
Device class
Class II
Review panel
Microbiology
Applicant
Clever Culture Systems Seestrasse 204a, Bach, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code QQY

Trailing 12 months

FDA records hold no clearances under product code QQY in the trailing twelve months.

FDA records show no clearances under product code QQY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code QQY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260