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FDA 510(k)

I.D. AND SEAKEM GTG AGAROSES

K-Number: K940037 · 1995-02-24

ApplicantFmc Corp.
Decision Date1995-02-24
Product CodeJZR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

I.D. AND SEAKEM GTG AGAROSES is the device name listed in this FDA 510(k) record. The listed applicant is Fmc Corp.. It received FDA 510(k) clearance on 1995-02-24 under 510(k) number K940037. The device is classified under product code JZR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.D. AND SEAKEM GTG AGAROSES?

I.D. AND SEAKEM GTG AGAROSES is a medical device that received FDA 510(k) clearance on 1995-02-24. The listed applicant is Fmc Corp.. The 510(k) number is K940037.

When did I.D. AND SEAKEM GTG AGAROSES receive FDA 510(k) clearance?

I.D. AND SEAKEM GTG AGAROSES received FDA 510(k) clearance on 1995-02-24, under 510(k) number K940037.

Who is the listed applicant for I.D. AND SEAKEM GTG AGAROSES?

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 I.D. AND SEAKEM GTG AGAROSES?

The FDA product code for I.D. AND SEAKEM GTG AGAROSES is JZR.

Related Clinical Trials

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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.

K841407ISOGEL AGAROSE

Related Devices (Code: JZR)

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.

K831603TITAN GE/IEPLATEHelena 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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