FISIO CHAMBER SPACE
FDA 510(k) clearance K101136 · decided 2011-01-28
Clearance details
- K-number
- K101136
- Device name
- FISIO CHAMBER SPACE
- Applicant
- Koo (Shanghai) Industries Co., Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2010-04-22
- Decision date
- 2011-01-28
- Days to decision
- 281 days
- Clearance type
- Traditional
- Product code
- NVP
- Device class
- 2
- Regulation number
- 868.5630
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Bonita Springs, FL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Koo (Shanghai) Industries Co.
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.