KAWASUMI A.V. FISTULA SET— 510(k) K873421
Substantially EquivalentKawasumi Laboratories Co., Ltd.
FDA 510(k) clearance K873421 for KAWASUMI A.V. FISTULA SET, Substantially Equivalent on 1987-10-09. Applicant: Kawasumi Laboratories Co., Ltd..
Clearance details
- Applicant
- Kawasumi Laboratories Co., Ltd.
- Product code
- Code FKQ
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Canoga Park, CA, US
Adverse events under product code FKQ
product code FKQ- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.