.9% NORMAL SALINE TUBE/STERILE WATER TUBE
K-Number: K926405 · 1994-02-03
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Device Summary
Frequently Asked Questions
What is the .9% NORMAL SALINE TUBE/STERILE WATER TUBE?
.9% NORMAL SALINE TUBE/STERILE WATER TUBE is a medical device that received FDA 510(k) clearance on 1994-02-03. The listed applicant is Gam-Med Packaging Corp.. The 510(k) number is K926405.
When did .9% NORMAL SALINE TUBE/STERILE WATER TUBE receive FDA 510(k) clearance?
.9% NORMAL SALINE TUBE/STERILE WATER TUBE received FDA 510(k) clearance on 1994-02-03, under 510(k) number K926405.
Who is the listed applicant for .9% NORMAL SALINE TUBE/STERILE WATER TUBE?
The FDA 510(k) record lists Gam-Med Packaging Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for .9% NORMAL SALINE TUBE/STERILE WATER TUBE?
The FDA product code for .9% NORMAL SALINE TUBE/STERILE WATER TUBE 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.
Other records listing Gam-Med Packaging 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.
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.
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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