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FDA 510(k)

LIO-714 OPACITYMETER

K-Number: K790526 · 1979-11-16

ApplicantLaser Industries , Ltd.
Decision Date1979-11-16
Product CodeHJL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LIO-714 OPACITYMETER is the device name listed in this FDA 510(k) record. The listed applicant is Laser Industries , Ltd.. It received FDA 510(k) clearance on 1979-11-16 under 510(k) number K790526. The device is classified under product code HJL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIO-714 OPACITYMETER?

LIO-714 OPACITYMETER is a medical device that received FDA 510(k) clearance on 1979-11-16. The listed applicant is Laser Industries , Ltd.. The 510(k) number is K790526.

When did LIO-714 OPACITYMETER receive FDA 510(k) clearance?

LIO-714 OPACITYMETER received FDA 510(k) clearance on 1979-11-16, under 510(k) number K790526.

Who is the listed applicant for LIO-714 OPACITYMETER?

The FDA 510(k) record lists Laser Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIO-714 OPACITYMETER?

The FDA product code for LIO-714 OPACITYMETER is HJL.

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Other records listing Laser Industries , Ltd. 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.

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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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