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FDA 510(k)

.9% NORMAL SALINE TUBE/STERILE WATER TUBE

K-Number: K926405 · 1994-02-03

Decision Date1994-02-03
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

.9% NORMAL SALINE TUBE/STERILE WATER TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Gam-Med Packaging Corp.. It received FDA 510(k) clearance on 1994-02-03 under 510(k) number K926405. 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 .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

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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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