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FDA 510(k)

OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190

K-Number: K123365 · 2013-03-01

Decision Date2013-03-01
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2013-03-01 under 510(k) number K123365. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190?

OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190 is a medical device that received FDA 510(k) clearance on 2013-03-01. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K123365.

When did OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190 receive FDA 510(k) clearance?

OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190 received FDA 510(k) clearance on 2013-03-01, under 510(k) number K123365.

Who is the listed applicant for OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190?

The FDA 510(k) record lists Olympus Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190?

The FDA product code for OLYMPUS LTF-190-10-3D, MAJ-Y0154, OLYMPUS CV-190 is HET.

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.

Other records listing Olympus Medical Systems Corp. 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.

View all 97 devices →

Related Devices (Code: HET)

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

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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