SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES— 510(k) K891879
Substantially EquivalentSumma Intl.
FDA 510(k) clearance K891879 for SUMMA PROTECH: DELTA SERIES PATIENT EXAM GLOVES, Substantially Equivalent on 1989-06-06. Applicant: Summa Intl..
Clearance details
- Applicant
- Summa Intl.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Phoenix, AZ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.