ClearanceBrief
Company ยท US

Kinetic Technology, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1988 to 1992. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LXMManipulator, Plunger-Like Joint5

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 30, 1992K922695KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5
Kinetic Technology, Inc.
LXM
Sep 30, 1992K922694KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4
Kinetic Technology, Inc.
LXM
Sep 30, 1992K922693KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1
Kinetic Technology, Inc.
LXM
Sep 30, 1992K922692KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR
Kinetic Technology, Inc.
LXM
Apr 26, 1988K870910PRECISION SPINAL ADJUSTER MODEL 115
Kinetic Technology, Inc.
LXM

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes