K840565Substantially Equivalent
Monitor 5590- Analyzer 5595Ec
Hudson Oxygen Therapy Sales Co., Mchenry IL / Traditional, Substantially Equivalent
K840565 is the FDA 510(k) clearance record for MONITOR 5590- ANALYZER 5595EC, a class II device, cleared for Hudson Oxygen Therapy Sales Co. on under FDA product code CCL (Analyzer, Gas, Oxygen, Gaseous-Phase). FDA records list 33 510(k) clearances for Hudson Oxygen Therapy Sales Co., from to . As of , FDA records show no recalls naming K840565.
Clearance record
- Decision date
- Received
- (54 days to decision)
- Product code
- CCL Analyzer, Gas, Oxygen, Gaseous-Phase
- Regulation
- 21 CFR 868.1720
- Device class
- Class II
- Review panel
- Anesthesiology
- Applicant
- Hudson Oxygen Therapy Sales Co. 803 N. Front St. Suite 3, Mchenry IL
- Third party review
- No
Clearances, product code CCL
Trailing 12 monthsShow 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 | 1 |
| 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.
