FDA 510(k)

OCULAR PRESSURE APPLICATOR

K-Number: K841652 · 1984-06-01

Decision Date1984-06-01

Product Code

DecisionSubstantially Equivalent

Device Summary

OCULAR PRESSURE APPLICATOR is the device name listed in this FDA 510(k) record. The listed applicant is The Lebanon Corp.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K841652. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCULAR PRESSURE APPLICATOR?

OCULAR PRESSURE APPLICATOR is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is The Lebanon Corp.. The 510(k) number is K841652.

When did OCULAR PRESSURE APPLICATOR receive FDA 510(k) clearance?

OCULAR PRESSURE APPLICATOR received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841652.

Who is the listed applicant for OCULAR PRESSURE APPLICATOR?

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

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing The Lebanon Corp. as applicant

K821689LEBANON MICROSCOPE K820526RELIEF VALVE-HONAN INTRAOC. PRESSURE

Official Source

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