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FDA 510(k)

VIBROMETRY SYSTEM

K-Number: K901881 · 1991-05-31

ApplicantBruel & Kjaer Instruments, Inc.
Decision Date1991-05-31
Product CodeLNN
DecisionSubstantially Equivalent

Device Summary

VIBROMETRY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bruel & Kjaer Instruments, Inc.. It received FDA 510(k) clearance on 1991-05-31 under 510(k) number K901881. The device is classified under product code LNN. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBROMETRY SYSTEM?

VIBROMETRY SYSTEM is a medical device that received FDA 510(k) clearance on 1991-05-31. The listed applicant is Bruel & Kjaer Instruments, Inc.. The 510(k) number is K901881.

When did VIBROMETRY SYSTEM receive FDA 510(k) clearance?

VIBROMETRY SYSTEM received FDA 510(k) clearance on 1991-05-31, under 510(k) number K901881.

Who is the listed applicant for VIBROMETRY SYSTEM?

The FDA 510(k) record lists Bruel & Kjaer Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIBROMETRY SYSTEM?

The FDA product code for VIBROMETRY SYSTEM is LNN.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Bruel & Kjaer Instruments, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890446ANESTHETIC GAS MONITORK827409REAL TIME ULTRASOUND SCANNER 1849K827380SCANNER TYPE 1846

Related Devices (Code: LNN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K932342MODEL 500-6 RADIATION THERAPY IONIZATION CHAMBERVictoreen, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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