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FDA 510(k)

OLYMPUS LACTATE, OSR6193

K-Number: K042406 · 2004-12-03

ApplicantOlympus America, Inc.
Decision Date2004-12-03
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

OLYMPUS LACTATE, OSR6193 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus America, Inc.. It received FDA 510(k) clearance on 2004-12-03 under 510(k) number K042406. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS LACTATE, OSR6193?

OLYMPUS LACTATE, OSR6193 is a medical device that received FDA 510(k) clearance on 2004-12-03. The listed applicant is Olympus America, Inc.. The 510(k) number is K042406.

When did OLYMPUS LACTATE, OSR6193 receive FDA 510(k) clearance?

OLYMPUS LACTATE, OSR6193 received FDA 510(k) clearance on 2004-12-03, under 510(k) number K042406.

Who is the listed applicant for OLYMPUS LACTATE, OSR6193?

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

What is the FDA product code for OLYMPUS LACTATE, OSR6193?

The FDA product code for OLYMPUS LACTATE, OSR6193 is JIT.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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