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FDA 510(k)

STERILE WATER O.9% STERILE SALINE

K-Number: K954887 · 1996-01-24

ApplicantLockett Medical Corp.
Decision Date1996-01-24
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE WATER O.9% STERILE SALINE is the device name listed in this FDA 510(k) record. The listed applicant is Lockett Medical Corp.. It received FDA 510(k) clearance on 1996-01-24 under 510(k) number K954887. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE WATER O.9% STERILE SALINE?

STERILE WATER O.9% STERILE SALINE is a medical device that received FDA 510(k) clearance on 1996-01-24. The listed applicant is Lockett Medical Corp.. The 510(k) number is K954887.

When did STERILE WATER O.9% STERILE SALINE receive FDA 510(k) clearance?

STERILE WATER O.9% STERILE SALINE received FDA 510(k) clearance on 1996-01-24, under 510(k) number K954887.

Who is the listed applicant for STERILE WATER O.9% STERILE SALINE?

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

What is the FDA product code for STERILE WATER O.9% STERILE SALINE?

The FDA product code for STERILE WATER O.9% STERILE SALINE is FOZ.

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 Lockett Medical 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.

K011176REUSABLE GLASS SYRINGESK950404LOCKETT MEDICAL CORP. GAUZE

Related Devices (Code: FOZ)

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.

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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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