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FDA 510(k)

HI CHEM ELECTROLYTE BUFFER

K-Number: K925612 · 1993-04-20

Decision Date1993-04-20
Product CodeJGS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HI CHEM ELECTROLYTE BUFFER is the device name listed in this FDA 510(k) record. The listed applicant is Hichem Diagnostics. It received FDA 510(k) clearance on 1993-04-20 under 510(k) number K925612. 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 HI CHEM ELECTROLYTE BUFFER?

HI CHEM ELECTROLYTE BUFFER is a medical device that received FDA 510(k) clearance on 1993-04-20. The listed applicant is Hichem Diagnostics. The 510(k) number is K925612.

When did HI CHEM ELECTROLYTE BUFFER receive FDA 510(k) clearance?

HI CHEM ELECTROLYTE BUFFER received FDA 510(k) clearance on 1993-04-20, under 510(k) number K925612.

Who is the listed applicant for HI CHEM ELECTROLYTE BUFFER?

The FDA 510(k) record lists Hichem Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HI CHEM ELECTROLYTE BUFFER?

The FDA product code for HI CHEM ELECTROLYTE BUFFER is JGS.

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 Hichem Diagnostics 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.

View all 41 devices →

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.

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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