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FDA 510(k)

POLARISED LIGHT GRONIOMETER

K-Number: K810640 · 1981-04-17

ApplicantCairco , Ltd.
Decision Date1981-04-17
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POLARISED LIGHT GRONIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Cairco , Ltd.. It received FDA 510(k) clearance on 1981-04-17 under 510(k) number K810640. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLARISED LIGHT GRONIOMETER?

POLARISED LIGHT GRONIOMETER is a medical device that received FDA 510(k) clearance on 1981-04-17. The listed applicant is Cairco , Ltd.. The 510(k) number is K810640.

When did POLARISED LIGHT GRONIOMETER receive FDA 510(k) clearance?

POLARISED LIGHT GRONIOMETER received FDA 510(k) clearance on 1981-04-17, under 510(k) number K810640.

Who is the listed applicant for POLARISED LIGHT GRONIOMETER?

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

What is the FDA product code for POLARISED LIGHT GRONIOMETER?

The FDA product code for POLARISED LIGHT GRONIOMETER is KQX.

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Other records listing Cairco , Ltd. as applicant

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Related Devices (Code: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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