MOVIT DEVICE
FDA 510(k) clearance K921710 · decided 1992-06-29
Clearance details
- K-number
- K921710
- Device name
- MOVIT DEVICE
- Applicant
- John J. Navar, M.D.
- Decision
- Substantially Equivalent
- Date received
- 1992-04-08
- Decision date
- 1992-06-29
- Days to decision
- 82 days
- Clearance type
- Traditional
- Product code
- BRY
- Device class
- 1
- Regulation number
- 868.6100
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- Location
- Corpus Christi, TX, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch John J. Navar
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.
| Record | Firm | Date |
|---|---|---|
| MEDIKEEPER (K912346) | Medikeeper, Inc. | 1991-07-30 |
| ANESTHESIA WORKSTATION (K901474) | Siemens Life Support Systems | 1990-04-10 |
| ANESTHASSIST (K871564) | Anestech, Inc. | 1987-05-18 |
| ANESTHECACHE (K821307) | Med-Life, Inc. | 1982-05-14 |
Recalls involving this device
No recalls on record reference this clearance.