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FDA 510(k)

LEBANON MICROSCOPE

K-Number: K821689 · 1982-07-09

ApplicantThe Lebanon Corp.
Decision Date1982-07-09
Product CodeEPT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LEBANON MICROSCOPE 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 1982-07-09 under 510(k) number K821689. The device is classified under product code EPT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEBANON MICROSCOPE?

LEBANON MICROSCOPE is a medical device that received FDA 510(k) clearance on 1982-07-09. The listed applicant is The Lebanon Corp.. The 510(k) number is K821689.

When did LEBANON MICROSCOPE receive FDA 510(k) clearance?

LEBANON MICROSCOPE received FDA 510(k) clearance on 1982-07-09, under 510(k) number K821689.

Who is the listed applicant for LEBANON MICROSCOPE?

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

What is the FDA product code for LEBANON MICROSCOPE?

The FDA product code for LEBANON MICROSCOPE is EPT.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing The Lebanon 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.

K841652OCULAR PRESSURE APPLICATORK820526RELIEF VALVE-HONAN INTRAOC. PRESSURE

Related Devices (Code: EPT)

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.

K942233MKM (MULTIPLE COORDINATE MANIPULATOR) SYSTEMCarl Zeiss, Inc.K931284MICRODYNE OFFICE SURGICAL MICROSCOPEMicrodyne, Inc.K933310MICRINS CONTRAST BACKGROUND MATERIALMicrins Surgical, Inc.K903412STORZ MODEL M705 AND/OR M706 CEILING MOUNTED MICR.Storz Instrument Co.K883581OPMI CSCarl Zeiss, Inc.K882269STORZ DIAGNOSTIC MICROSCOPE SYSTEMStorz Instrument Co.

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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