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FDA 510(k)

BIO-IMPEDANCE ANALYZER

K-Number: K904109 · 1991-01-08

Decision Date1991-01-08
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BIO-IMPEDANCE ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Xitron Technologies, Inc.. It received FDA 510(k) clearance on 1991-01-08 under 510(k) number K904109. The device is classified under product code DSB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-IMPEDANCE ANALYZER?

BIO-IMPEDANCE ANALYZER is a medical device that received FDA 510(k) clearance on 1991-01-08. The listed applicant is Xitron Technologies, Inc.. The 510(k) number is K904109.

When did BIO-IMPEDANCE ANALYZER receive FDA 510(k) clearance?

BIO-IMPEDANCE ANALYZER received FDA 510(k) clearance on 1991-01-08, under 510(k) number K904109.

Who is the listed applicant for BIO-IMPEDANCE ANALYZER?

The FDA 510(k) record lists Xitron Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-IMPEDANCE ANALYZER?

The FDA product code for BIO-IMPEDANCE ANALYZER is DSB.

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.

Related Devices (Code: DSB)

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.

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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