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.

Derata Corp.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K883847	DERATA MEDI-JECTOR V	KZE	1988-10-31	View
510(k)	K864561	DERATA MEDI-JECTOR IV	KZE	1987-02-19	View
510(k)	K844244	DERATA MEDI-JECTOR PRO	KZE	1985-07-05	View
510(k)	K844111	DERATA MEDI-JECTOR III	KZE	1984-11-28	View
510(k)	K834044	MEDI-JECTOR II	KZE	1984-03-06	View
510(k)	K772129	MEDI-JECTOR	KZE	1977-12-08	View

↑