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FDA 510(k)

NALGENE EMERGENCY EYE WASH

K-Number: K760820 · 1976-10-20

ApplicantNagle Co.
Decision Date1976-10-20
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NALGENE EMERGENCY EYE WASH is the device name listed in this FDA 510(k) record. The listed applicant is Nagle Co.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760820. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NALGENE EMERGENCY EYE WASH?

NALGENE EMERGENCY EYE WASH is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Nagle Co.. The 510(k) number is K760820.

When did NALGENE EMERGENCY EYE WASH receive FDA 510(k) clearance?

NALGENE EMERGENCY EYE WASH received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760820.

Who is the listed applicant for NALGENE EMERGENCY EYE WASH?

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

What is the FDA product code for NALGENE EMERGENCY EYE WASH?

The FDA product code for NALGENE EMERGENCY EYE WASH is KYG.

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

Related Devices (Code: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, 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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