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FDA 510(k)

ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT.

K-Number: K882104 · 1988-07-05

ApplicantParamax Systems Div. Baxter Healthcare
Decision Date1988-07-05
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT. is the device name listed in this FDA 510(k) record. The listed applicant is Paramax Systems Div. Baxter Healthcare. It received FDA 510(k) clearance on 1988-07-05 under 510(k) number K882104. The device is classified under product code JGS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT.?

ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT. is a medical device that received FDA 510(k) clearance on 1988-07-05. The listed applicant is Paramax Systems Div. Baxter Healthcare. The 510(k) number is K882104.

When did ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT. receive FDA 510(k) clearance?

ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT. received FDA 510(k) clearance on 1988-07-05, under 510(k) number K882104.

Who is the listed applicant for ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT.?

The FDA 510(k) record lists Paramax Systems Div. Baxter Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT.?

The FDA product code for ION SELECTIVE ELECTRODE SUBSYSTEM OF PARA. ANALYT. is JGS.

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Related Devices (Code: JGS)

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.

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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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