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FDA 510(k)

PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX

K-Number: K901141 · 1990-04-09

ApplicantBaxter Healthcare Corp
Decision Date1990-04-09
Product CodeJJC
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX 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 1990-04-09 under 510(k) number K901141. The device is classified under product code JJC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX?

PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX is a medical device that received FDA 510(k) clearance on 1990-04-09. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K901141.

When did PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX receive FDA 510(k) clearance?

PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX received FDA 510(k) clearance on 1990-04-09, under 510(k) number K901141.

Who is the listed applicant for PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX?

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 520, PARAMAX 720 AND PARAMAX 720ZX?

The FDA product code for PARAMAX 520, PARAMAX 720 AND PARAMAX 720ZX is JJC.

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Other records listing Baxter Healthcare Corp as applicant

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Related Devices (Code: JJC)

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.

K945915AVL OMNI ANALYZERAvl Scientific Corp.K945584NOVA 16 ANALYZERNova Biomedical Corp.K943376OPERA SYSTEMMiles, Inc.K901410TECHNICON RA-2000(TM) SYSTEMTechnicon Instruments Corp.K890332RFA/2 RAPID FLOW ANALYZER W/COMPUTERAlpkem Corp.K881056AMRESCO FLOW PAC RANDOM ACCESS LIQUID #4901030American Research Products Co.

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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