FDA 510(k)

BOD POD

K-Number: K060848 · 2006-06-27

Decision Date2006-06-27

Product CodeOAC

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

BOD POD is the device name listed in this FDA 510(k) record. The listed applicant is Life Measurement, Inc.. It received FDA 510(k) clearance on 2006-06-27 under 510(k) number K060848. The device is classified under product code OAC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOD POD?

BOD POD is a medical device that received FDA 510(k) clearance on 2006-06-27. The listed applicant is Life Measurement, Inc.. The 510(k) number is K060848.

When did BOD POD receive FDA 510(k) clearance?

BOD POD received FDA 510(k) clearance on 2006-06-27, under 510(k) number K060848.

Who is the listed applicant for BOD POD?

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

What is the FDA product code for BOD POD?

The FDA product code for BOD POD is OAC.

Other records listing Life Measurement, 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.

K032610MODIFIED SONAMET BODY COMPOSITION ANALYZER

Related Devices (Code: OAC)

K032610MODIFIED SONAMET BODY COMPOSITION ANALYZERLife Measurement, Inc.K924972SONAMET BODY COMPOSITION ANALYZERLife Measurement Instruments, 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.