The following data is part of a premarket notification filed by Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. with the FDA for Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You..
| Device ID | K222225 |
| 510k Number | Error Temporarily Unavailable |
| Device Name: | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Classification | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Applicant | #Error.diagnostics# |
| Contact | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Correspondent | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. #Error.diagnostics# |
| Product Code | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| CFR Regulation Number | Error Temporarily Unavailable [🔎] |
| Decision | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Type | Error Temporari |
| 3rd Party Reviewed | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Combination Product | Error Temporarily Unavailable Please Select Your Back Button Or Choose A Page Listed Below. Thank You. |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20860011916608 | K222225 | 000 |
| 20860011820196 | K222225 | 000 |
| 20860011820189 | K222225 | 000 |
| 20860011820172 | K222225 | 000 |
| 20860011820165 | K222225 | 000 |