Regulations.gov document
Attachment 4 Device Comparison with Approved 510k Needle Based Devices re Petition for…
Supporting & Related Material · FDA-2019-P-2124 · posted May 3, 2019
Key facts
| Document ID | FDA-2019-P-2124-0007 |
|---|---|
| Title | Attachment 4 Device Comparison with Approved 510k Needle Based Devices re Petition for Administrative Reconsideration from C Laser Inc. |
| Document type | Supporting & Related Material |
| Subtype | Background Material |
| Agency | FDA |
| Docket | FDA-2019-P-2124 |
| Posted | May 3, 2019 |
At a glance
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