PYLORAGEN HELICBACTER PYLORI TEST KIT - MODIFIED— 510(k) K923445
Substantially EquivalentHycor Biomedical, Inc.
FDA 510(k) clearance K923445 for PYLORAGEN HELICBACTER PYLORI TEST KIT - MODIFIED, Substantially Equivalent on 1992-09-11. Applicant: Hycor Biomedical, Inc..
Clearance details
- Applicant
- Hycor Biomedical, Inc.
- Product code
- Code LYR
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Garden Grove, CA, US
Adverse events under product code LYR
product code LYR- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.