FLEXI-TRAK(TM) ANCHORING DEVICE— 510(k) K905128
Substantially EquivalentConvatec, A Division of E.R. Squibb & Sons
FDA 510(k) clearance K905128 for FLEXI-TRAK(TM) ANCHORING DEVICE, Substantially Equivalent on 1990-11-29. Applicant: Convatec, A Division of E.R. Squibb & Sons.
Clearance details
- Applicant
- Convatec, A Division of E.R. Squibb & Sons
- Product code
- Code KNY
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Princeton, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.