ClearanceBrief
Company ยท US

Kemble Instruments, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1984. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
JJJCounter (Beta, Gamma) For Clinical Use6
JQPCalculator/Data Processing Module, For Clinical Use1
JQWStation, Pipetting And Diluting, For Clinical Use1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 27, 1984K842894KEMBLE 405
Kemble Instruments, Inc.
JQW
Oct 14, 1983K832760RIA SOFTWARE
Kemble Instruments, Inc.
JQP
Oct 14, 1983K832734KEMTEK 400 RIA GAMMA COUNTER
Kemble Instruments, Inc.
JJJ
Sep 29, 1983K832736KEMTEK 104 RIA GAMMA COUNTER
Kemble Instruments, Inc.
JJJ
Sep 29, 1983K832735KEMTEK 103 RIA GAMMA COUNTER
Kemble Instruments, Inc.
JJJ
Apr 6, 1983K830751KEMTEK 102
Kemble Instruments, Inc.
JJJ
Aug 24, 1982K822293IMMU-COUNT 404
Kemble Instruments, Inc.
JJJ
Aug 16, 1982K827748THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE
Kemble Instruments, Inc.
Feb 5, 1982K820137IMMU-COUNT
Kemble Instruments, Inc.
JJJ

Latest recalls

DateFirm and productCodeLinked 510(k)
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