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FDA 510(k)

ELECTROPHORESIS TANK

K-Number: K924020 · 1992-12-28

ApplicantThe Binding Site, Ltd.
Decision Date1992-12-28
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ELECTROPHORESIS TANK is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site, Ltd.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K924020. The device is classified under product code JJN. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTROPHORESIS TANK?

ELECTROPHORESIS TANK is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K924020.

When did ELECTROPHORESIS TANK receive FDA 510(k) clearance?

ELECTROPHORESIS TANK received FDA 510(k) clearance on 1992-12-28, under 510(k) number K924020.

Who is the listed applicant for ELECTROPHORESIS TANK?

The FDA 510(k) record lists The Binding Site, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECTROPHORESIS TANK?

The FDA product code for ELECTROPHORESIS TANK is JJN.

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Other records listing The Binding Site, Ltd. as applicant

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Related Devices (Code: JJN)

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.

K924021POWER SUPPLYThe Binding Site, Ltd.K882344ELECTR-TRANSBLOTTERThe W.E.P. Co.K881852REP SP ELECTROPHORESIS SYSTEM CAT NO. 3170Helena LaboratoriesK882163HELENA REP GEL PROCESSORHelena LaboratoriesK873352RAPID ELECTROPHORESIS SYSTEM (REP)Helena LaboratoriesK864436STAVIP 3000Roseburg SA

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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