CATHETER VALVES KV 100 & KV 100EH
FDA 510(k) clearance K861699 · decided 1986-11-19
Clearance details
- K-number
- K861699
- Device name
- CATHETER VALVES KV 100 & KV 100EH
- Applicant
- Max Staubli , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1986-05-05
- Decision date
- 1986-11-19
- Days to decision
- 198 days
- Clearance type
- Traditional
- Product code
- KOD
- Device class
- 2
- Regulation number
- 876.5130
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Horgen, Switzerland, CH
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Max Staubli
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.