Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FHC, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2023-09-08
TypeNumberDevice NameCodeDateActions
510(k) K231141 STarFix Designer Software C0265QRI2023-09-08 View
510(k) K200169 VFS1 Bipolar Electrosurgical GeneratorGEI2020-05-14 View
510(k) K183123 microTargeting Guideline 4000 5.0 SystemGZL2018-12-20 View
↑