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Cyberex Corp. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

No warning letters matched by name

Inspections 0 0 OAI

Recalls 0 0 Class I

Warning letters 0 None on file

510(k) clearances 4 Latest May 5, 1981

Cyberex Corp. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Cyberex Corp." is on file.

What these totals cover: FDA records filed under the name "Cyberex Corp." and its spelling variant "Cyberex".

Latest 510(k): May 5, 1981

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 11, 2026 (checked Nov 15, 2026, unchanged)	File dated Nov 10, 2026	Current
510(k) clearances	4	Nov 15, 2026	File dated Nov 9, 2026	Current
Inspections	0	Nov 15, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Recent 510(k) clearances

4 510(k) clearances from Jun 27, 1979 to May 5, 1981.

K-Number	Device	Date
K810837	CYBER 80 HEMODIALYZER	May 5, 1981
K802478	CYBER 120 HEMODIALYZER	Mar 20, 1981
K801377	CYBER 120 HEMODIALYZER	Aug 27, 1980
K790824	REPGREEN ULTRAFILTRATION MONITOR	Jun 27, 1979

Cyberex Corp. and the FDA: common questions

Has Cyberex Corp. received an FDA warning letter?

No FDA warning letter addressed to the name "Cyberex Corp." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Cyberex Corp. received an FDA Form 483?

FDA has not published a Form 483 for "Cyberex Corp." in its reading room. FDA publishes some Form 483s, not all of them.

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