SODIUM CHLORIDE SOLUTION
K-Number: K903347 · 1990-12-13
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Device Summary
Frequently Asked Questions
What is the SODIUM CHLORIDE SOLUTION?
SODIUM CHLORIDE SOLUTION is a medical device that received FDA 510(k) clearance on 1990-12-13. The listed applicant is Superior Healthcare Group, Inc.. The 510(k) number is K903347.
When did SODIUM CHLORIDE SOLUTION receive FDA 510(k) clearance?
SODIUM CHLORIDE SOLUTION received FDA 510(k) clearance on 1990-12-13, under 510(k) number K903347.
Who is the listed applicant for SODIUM CHLORIDE SOLUTION?
The FDA 510(k) record lists Superior Healthcare Group, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SODIUM CHLORIDE SOLUTION?
The FDA product code for SODIUM CHLORIDE SOLUTION 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 Superior Healthcare Group, Inc. 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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