CUTTER POINTS
FDA 510(k) clearance K792250 · decided 1980-01-23
Clearance details
- K-number
- K792250
- Device name
- CUTTER POINTS
- Applicant
- Cutter Laboratories, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-11-08
- Decision date
- 1980-01-23
- Days to decision
- 76 days
- Clearance type
- Traditional
- Product code
- EHL
- Device class
- 1
- Regulation number
- 872.6010
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Cutter Laboratories
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 |
|---|---|---|
| DENTAL ABRASIVE DEVICE (K780811) | Cavitron Corp. | 1978-06-22 |
| MINIDENTOFLEX NEW POLISHING SYSTEM (K780376) | Cavitron Corp. | 1978-03-14 |
| PINIDENTOFLEX DENTAL POLISHER (K780377) | Cavitron Corp. | 1978-03-14 |
Recalls involving this device
No recalls on record reference this clearance.