510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901881Substantially Equivalent

Vibrometry System

Bruel & Kjaer Instruments, Inc., Hoffman Estates IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901881 is the FDA 510(k) clearance record for VIBROMETRY SYSTEM, cleared for Bruel & Kjaer Instruments, Inc. on under FDA product code LNN. FDA records list 4 510(k) clearances for Bruel & Kjaer Instruments, Inc., from to . As of , FDA records show no recalls naming K901881.

Clearance record

Decision date
Received
(400 days to decision)
Product code
LNN
Review panel
Unknown
Applicant
Bruel & Kjaer Instruments, Inc. 555 W. Central Rd., Hoffman Estates IL
Third party review
No

Clearances, product code LNN

Trailing 12 months

FDA records hold no clearances under product code LNN in the trailing twelve months.

FDA records show no clearances under product code LNN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LNN, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260