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FDA 510(k)

LINEAR CLOUD TONOMETER

K-Number: K841089 · 1984-05-22

Decision Date1984-05-22
Product CodeLCH
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LINEAR CLOUD TONOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Linear Tonometers, Inc.. It received FDA 510(k) clearance on 1984-05-22 under 510(k) number K841089. The device is classified under product code LCH. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINEAR CLOUD TONOMETER?

LINEAR CLOUD TONOMETER is a medical device that received FDA 510(k) clearance on 1984-05-22. The listed applicant is Linear Tonometers, Inc.. The 510(k) number is K841089.

When did LINEAR CLOUD TONOMETER receive FDA 510(k) clearance?

LINEAR CLOUD TONOMETER received FDA 510(k) clearance on 1984-05-22, under 510(k) number K841089.

Who is the listed applicant for LINEAR CLOUD TONOMETER?

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

What is the FDA product code for LINEAR CLOUD TONOMETER?

The FDA product code for LINEAR CLOUD TONOMETER is LCH.

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.

Related Devices (Code: LCH)

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

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