FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G
K-Number: K850127 · 1985-03-20
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Device Summary
Frequently Asked Questions
What is the FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G?
FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Computer Dialysis Systems, Inc.. The 510(k) number is K850127.
When did FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G receive FDA 510(k) clearance?
FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850127.
Who is the listed applicant for FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G?
The FDA 510(k) record lists Computer Dialysis Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G?
The FDA product code for FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G is LIF.
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 Computer Dialysis Systems, 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: LIF)
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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