SUCTION WOUND DRAINAGE DEVICE— 510(k) K810739
Substantially EquivalentThe Urology Group
FDA 510(k) clearance K810739 for SUCTION WOUND DRAINAGE DEVICE, Substantially Equivalent on 1981-06-26. Applicant: The Urology Group.
Clearance details
- Applicant
- The Urology Group
- Product code
- Code KQT
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.