PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891979
Substantially EquivalentJeanine Alcantara Intl.
FDA 510(k) clearance K891979 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-04-28. Applicant: Jeanine Alcantara Intl..
Clearance details
- Applicant
- Jeanine Alcantara Intl.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.