ARTHROPHONOMETER
FDA 510(k) clearance K862286 · decided 1987-01-07
Clearance details
- K-number
- K862286
- Device name
- ARTHROPHONOMETER
- Applicant
- Arthrotek, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1986-06-16
- Decision date
- 1987-01-07
- Days to decision
- 205 days
- Clearance type
- Traditional
- Product code
- NFQ
- Device class
- 1
- Regulation number
- 872.2050
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- West Hartford, CT, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Arthrotek
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 |
|---|---|---|
| ESG-1 ELECTROSONOGRAM (ESG-1) (K970116) | Myo-Tronics, Inc. | 1997-04-02 |
| SONOPAK/QS, SONOPAK (K905657) | Bioresearch | 1991-05-15 |
| ELECTROSONOGRAM ESG-1 (K905449) | Myo-Tronics, Inc. | 1991-04-26 |
Recalls involving this device
No recalls on record reference this clearance.