FDA 510(k) Applications Submitted by PERIMED, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990960 | 03/22/1999 | PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040) | PERIMED, INC. |
| K974285 | 11/14/1997 | PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT | PERIMED, INC. |
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