FDA 510(k)

SCANNER TYPE 1846

K-Number: K827380 · 1982-07-09

ApplicantBruel & Kjaer Instruments, Inc.

Decision Date1982-07-09

Product Code

DecisionSubstantially Equivalent

Device Summary

SCANNER TYPE 1846 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 1982-07-09 under 510(k) number K827380. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANNER TYPE 1846?

SCANNER TYPE 1846 is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is Bruel & Kjaer Instruments, Inc.. The 510(k) number is K827380.

When did SCANNER TYPE 1846 receive FDA 510(k) clearance?

SCANNER TYPE 1846 received FDA 510(k) clearance on 1982-07-09, under 510(k) number K827380.

Who is the listed applicant for SCANNER TYPE 1846?

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

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

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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.