THE ADVENTURER
FDA 510(k) clearance K881410 · decided 1988-04-21
Clearance details
- K-number
- K881410
- Device name
- THE ADVENTURER
- Applicant
- Westport Mobility Products, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1988-04-04
- Decision date
- 1988-04-21
- Days to decision
- 17 days
- Clearance type
- Traditional
- Product code
- IOR
- Device class
- 1
- Regulation number
- 890.3850
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- Canada, CA
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Westport Mobility Products
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.