PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891980
Substantially EquivalentMontrose Intl., Corp.
FDA 510(k) clearance K891980 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-04-28. Applicant: Montrose Intl., Corp..
Clearance details
- Applicant
- Montrose Intl., Corp.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.