PYQClass II
Rfid Chip For Dental Appliance
21 CFR 880.6300 / General Hospital
PYQ is the FDA product code for Rfid Chip For Dental Appliance, a class II device type, regulated under 21 CFR 880.6300. FDA's definition for this code reads: "The device is intended to enable access to secure patient identification and device information when used with complete dentures, partial dentures, and other removable oral appliances". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.
Classification record
- Product code
- PYQ
- Device name
- Rfid Chip For Dental Appliance
- FDA definition
- The device is intended to enable access to secure patient identification and device information when used with complete dentures, partial dentures, and other removable oral appliances.
- Regulation
- 21 CFR 880.6300
- Device class
- Class II
- Review panel
- General Hospital
- Submission type
- 510(k) exempt
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 1
- Ingested recalls
- 0
Clearances, product code PYQ
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 2017 | 1 |
Applicants with the most clearances
Product code PYQ| Applicant | Clearances |
|---|---|
| Cmp Industries, LLC | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeNo registered establishment in MDM’s records lists product code PYQ.
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