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FDA 510(k)

LIFELOG(TM)

K-Number: K902962 · 1990-09-04

ApplicantModular Instruments, Inc.
Decision Date1990-09-04
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFELOG(TM) is the device name listed in this FDA 510(k) record. The listed applicant is Modular Instruments, Inc.. It received FDA 510(k) clearance on 1990-09-04 under 510(k) number K902962. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFELOG(TM)?

LIFELOG(TM) is a medical device that received FDA 510(k) clearance on 1990-09-04. The listed applicant is Modular Instruments, Inc.. The 510(k) number is K902962.

When did LIFELOG(TM) receive FDA 510(k) clearance?

LIFELOG(TM) received FDA 510(k) clearance on 1990-09-04, under 510(k) number K902962.

Who is the listed applicant for LIFELOG(TM)?

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

What is the FDA product code for LIFELOG(TM)?

The FDA product code for LIFELOG(TM) is BSZ.

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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.

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