VIBROMETRY SYSTEM

K Number: K901881 · Decision May 31, 1991

Classifications

FEI Numbers

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Same Product Code

Applicant Total

Review Days

400

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Other 510(k) clearances with the same product code (LNN), ordered by most recent decision date.

K Number	Device Name	Decision Date	Decision
K890446	ANESTHETIC GAS MONITOR	Aug 11, 1989	Substantially Equivalent
K827409	REAL TIME ULTRASOUND SCANNER 1849	Jul 9, 1982	Substantially Equivalent
K827380	SCANNER TYPE 1846	Jul 9, 1982	Substantially Equivalent

This FDA 510(k) entry is associated with 0 FEI numbers. Click on an entry to view related FDA registrations.

This FDA 510(k) entry is associated with 0 registration numbers. Click on an entry to view related FDA registrations.

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Applicant

Bruel & Kjaer Instruments, Inc.

Product Code

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