Product code JYK
- Device name
- Holder, Ear Speculum
- Medical specialty
- General, Plastic Surgery
- Device class
- 1
- Regulation number
- 878.1800
- Review panel
- SU
- Implant
- N
- Life sustaining/supporting
- N
- GMP exempt
- N
- Third party review
- N
- Summary malfunction reporting
- Eligible
- Source
- FDA openFDA device classification dataset
Related 510(k) Records#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K822011 | SHEA'S EAR SPECULUM HOLDER PORT MANNS | Kelleher Corp. | 1982-08-12 |
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