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FDA 510(k)

PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK

K-Number: K903914 · 1990-10-03

ApplicantBaxter Healthcare Corp
Decision Date1990-10-03
Product CodeJGQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1990-10-03 under 510(k) number K903914. The device is classified under product code JGQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK?

PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK is a medical device that received FDA 510(k) clearance on 1990-10-03. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K903914.

When did PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK receive FDA 510(k) clearance?

PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK received FDA 510(k) clearance on 1990-10-03, under 510(k) number K903914.

Who is the listed applicant for PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK?

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 PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK?

The FDA product code for PARAMAX CEREBROSPINAL FLUID/URINE PROTEIN BLANK is JGQ.

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Related Devices (Code: JGQ)

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.

K131051HITACHI S TEST REAGENT CARTRIDGE TOTAL PROTEIN (TP) AND ALBUMIN (ALB)Hitachi Chemical Diagnostics, Inc.K072638ROCHE/HITACHI URINARY/CSF PROTEIN WITH MODEL(S) CAT #11877801Roche Diagnostics Corp.K071239TOTAL PROTEIN URINE/CSF GEN.3Roche DiagnosticsK981295UPROAbbott LaboratoriesK981682UPROAbbott LaboratoriesK925794TRACE MICROPROTEIN REAGENTTrace America, Inc.

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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