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FDA 510(k)

ISOGEL AGAROSE

K-Number: K841407 · 1985-07-16

ApplicantFmc Corp.
Decision Date1985-07-16
Product CodeJJN
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ISOGEL AGAROSE is the device name listed in this FDA 510(k) record. The listed applicant is Fmc Corp.. It received FDA 510(k) clearance on 1985-07-16 under 510(k) number K841407. 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 ISOGEL AGAROSE?

ISOGEL AGAROSE is a medical device that received FDA 510(k) clearance on 1985-07-16. The listed applicant is Fmc Corp.. The 510(k) number is K841407.

When did ISOGEL AGAROSE receive FDA 510(k) clearance?

ISOGEL AGAROSE received FDA 510(k) clearance on 1985-07-16, under 510(k) number K841407.

Who is the listed applicant for ISOGEL AGAROSE?

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

What is the FDA product code for ISOGEL AGAROSE?

The FDA product code for ISOGEL AGAROSE is JJN.

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.

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Other records listing Fmc Corp. 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.

K940037I.D. AND SEAKEM GTG AGAROSES

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.K924020ELECTROPHORESIS TANKThe 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 Laboratories

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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