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FDA 510(k)

MOIRE FRINGE VISOMETER AFTER LOTMAR

K-Number: K800238 · 1980-03-10

ApplicantHagg-Streit Service, Inc.
Decision Date1980-03-10
Product CodeHKL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MOIRE FRINGE VISOMETER AFTER LOTMAR is the device name listed in this FDA 510(k) record. The listed applicant is Hagg-Streit Service, Inc.. It received FDA 510(k) clearance on 1980-03-10 under 510(k) number K800238. The device is classified under product code HKL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOIRE FRINGE VISOMETER AFTER LOTMAR?

MOIRE FRINGE VISOMETER AFTER LOTMAR is a medical device that received FDA 510(k) clearance on 1980-03-10. The listed applicant is Hagg-Streit Service, Inc.. The 510(k) number is K800238.

When did MOIRE FRINGE VISOMETER AFTER LOTMAR receive FDA 510(k) clearance?

MOIRE FRINGE VISOMETER AFTER LOTMAR received FDA 510(k) clearance on 1980-03-10, under 510(k) number K800238.

Who is the listed applicant for MOIRE FRINGE VISOMETER AFTER LOTMAR?

The FDA 510(k) record lists Hagg-Streit Service, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOIRE FRINGE VISOMETER AFTER LOTMAR?

The FDA product code for MOIRE FRINGE VISOMETER AFTER LOTMAR is HKL.

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 Hagg-Streit Service, Inc. 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.

K882575DISTOMETER

Related Devices (Code: HKL)

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.

K001111PANORET, MODEL 1000ACmt Medical Technologies, Ltd.K950789STREAK RETINOSCOPE RX-1Neitz Instruments Company, Ltd.K950790STREAK RETINOSCOPE RX-2Neitz Instruments Company, Ltd.K893171VISTA STREAK RETINOSCOPE (AC-POWERED)Keeler Instruments, Inc.K812764KOI BLUE FIELD ENTOPTOSCOPEKoi, Inc.

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.

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