A-DEC 7284 CUSPIDOR, CASCADE
FDA 510(k) clearance K925367 · decided 1994-04-11
Clearance details
- K-number
- K925367
- Device name
- A-DEC 7284 CUSPIDOR, CASCADE
- Applicant
- A-Dec, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1992-10-21
- Decision date
- 1994-04-11
- Days to decision
- 537 days
- Clearance type
- Traditional
- Product code
- EBR
- Device class
- 1
- Regulation number
- 872.6640
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Newberg, OR, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch A-Dec
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 |
|---|---|---|
| DENPAX (K860058) | Nissho Iwai American Corp. | 1986-03-12 |
| OROPHARYNGEAL SUCTION AIRWAY (K770600) | W.H. Wall, D.D.S. | 1977-04-08 |
Recalls involving this device
No recalls on record reference this clearance.