K043543Substantially Equivalent
Blood Glucose Monitoring System
American Healthcare Corp., New York NY / Traditional, Substantially Equivalent
K043543 is the FDA 510(k) clearance record for BLOOD GLUCOSE MONITORING SYSTEM, a class II device, cleared for American Healthcare, Inc. on under FDA product code NBW (System, Test, Blood Glucose, Over The Counter). FDA records list 17 510(k) clearances for American Healthcare, Inc., from to . As of , FDA records show no recalls naming K043543.
Clearance record
- Decision date
- Received
- (109 days to decision)
- Product code
- NBW System, Test, Blood Glucose, Over The Counter
- Regulation
- 21 CFR 862.1345
- Device class
- Class II
- Review panel
- Clinical Chemistry
- Applicant
- American Healthcare, Inc. 304 Park Ave. S., Suite 218, New York NY
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NBW
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 | 1 |
| 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.
