Medical Device Manufacturer · US , Mchenry , IL

Peokin-Elmer Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1977
2
Total
2
Cleared
0
Denied

Peokin-Elmer Corp. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 2 cleared submissions from 1977 to 1977. Primary specialty: Toxicology.

Browse the FDA 510(k) cleared devices submitted by Peokin-Elmer Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Peokin-Elmer Corp.

2 devices
1-2 of 2
Cleared Jun 24, 1977
DETECTOR, UV, MOLEL GC-55
K770638 · KIE
Toxicology · 81d
Cleared Jun 24, 1977
DETECTOR, IR, MODEL GC-33
K770639 · KZQ
Toxicology · 81d
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