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FDA 510(k)

VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER

K-Number: K893963 · 1989-09-05

Decision Date1989-09-05
Product CodeDSB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is V.S.B.B. Technologies, Inc.. It received FDA 510(k) clearance on 1989-09-05 under 510(k) number K893963. 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 VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER?

VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER is a medical device that received FDA 510(k) clearance on 1989-09-05. The listed applicant is V.S.B.B. Technologies, Inc.. The 510(k) number is K893963.

When did VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER receive FDA 510(k) clearance?

VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER received FDA 510(k) clearance on 1989-09-05, under 510(k) number K893963.

Who is the listed applicant for VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER?

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

What is the FDA product code for VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER?

The FDA product code for VERIPOID 50 BIO-ELECTRICAL IMPEDANCE METER 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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