ClearanceBrief
Company ยท US

Derata Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1988. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KZEInjector, Fluid, Non-Electrically Powered6

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 31, 1988K883847DERATA MEDI-JECTOR V
Derata Corp.
KZE
Feb 19, 1987K864561DERATA MEDI-JECTOR IV
Derata Corp.
KZE
Jul 5, 1985K844244DERATA MEDI-JECTOR PRO
Derata Corp.
KZE
Nov 28, 1984K844111DERATA MEDI-JECTOR III
Derata Corp.
KZE
Mar 6, 1984K834044MEDI-JECTOR II
Derata Corp.
KZE
Dec 8, 1977K772129MEDI-JECTOR
Derata Corp.
KZE

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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