PULPDENT SNOOP
FDA 510(k) clearance K964430 · decided 1997-01-17
Clearance details
- K-number
- K964430
- Device name
- PULPDENT SNOOP
- Applicant
- Pulpdent Corp.
- Decision
- Substantially Equivalent
- Date received
- 1996-11-05
- Decision date
- 1997-01-17
- Days to decision
- 73 days
- Clearance type
- Traditional
- Product code
- LFC
- Device class
- 2
- Regulation number
- 872.1740
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Watertown, MA, US
- Third-party review
- No
- Expedited review
- No
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| CARIES FINDER (K955445) | Danville Engineering, Inc. | 1996-02-08 |
Recalls involving this device
No recalls on record reference this clearance.