0.9% SODIUM CHLORIDE FLUSH SYRINGE
K-Number: K984590 · 1999-10-07
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Device Summary
Frequently Asked Questions
What is the 0.9% SODIUM CHLORIDE FLUSH SYRINGE?
0.9% SODIUM CHLORIDE FLUSH SYRINGE is a medical device that received FDA 510(k) clearance on 1999-10-07. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K984590.
When did 0.9% SODIUM CHLORIDE FLUSH SYRINGE receive FDA 510(k) clearance?
0.9% SODIUM CHLORIDE FLUSH SYRINGE received FDA 510(k) clearance on 1999-10-07, under 510(k) number K984590.
Who is the listed applicant for 0.9% SODIUM CHLORIDE FLUSH SYRINGE?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 0.9% SODIUM CHLORIDE FLUSH SYRINGE?
The FDA product code for 0.9% SODIUM CHLORIDE FLUSH SYRINGE 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 Baxter Healthcare 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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