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510(k) K901881

VIBROMETRY SYSTEM by Bruel & Kjaer Instruments, Inc. — Product Code LNN

K901881 is an FDA 510(k) premarket notification submitted by Bruel & Kjaer Instruments, Inc. for the device "VIBROMETRY SYSTEM". The FDA issued a decision of Substantially Equivalent on May 31, 1991. Bruel & Kjaer Instruments, Inc. has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 31, 1991
Date Received
April 26, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Other clearances by Bruel & Kjaer Instruments, Inc.

  • K890446 — ANESTHETIC GAS MONITOR (August 11, 1989)
  • K827380 — SCANNER TYPE 1846 (July 9, 1982)
  • K827409 — REAL TIME ULTRASOUND SCANNER 1849 (July 9, 1982)

Other clearances for product code LNN

  • K932342 — MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBER (December 13, 1993)

FDA data resources