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FDA 510(k)

FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G

K-Number: K850127 · 1985-03-20

Decision Date1985-03-20
Product CodeLIF
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FORMA-TAG USP SODIUM CHLORIDE PACKAGE 80GM & 120 G is the device name listed in this FDA 510(k) record. The listed applicant is Computer Dialysis Systems, Inc.. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850127. The device is classified under product code LIF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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

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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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