APAS Independence with IC Chromogenic MRSA BD Analysis Module; APAS Independence with IC Chromogenic MRSA TFS/S Analysis Module
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 monthsFDA records hold no clearances under product code QQY in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
