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FDA 510(k)

C.A.T. REAGENT KIT

K-Number: K830322 · 1983-03-28

ApplicantRemel Co.
Decision Date1983-03-28
Product CodeJTQ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

C.A.T. REAGENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1983-03-28 under 510(k) number K830322. The device is classified under product code JTQ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.A.T. REAGENT KIT?

C.A.T. REAGENT KIT is a medical device that received FDA 510(k) clearance on 1983-03-28. The listed applicant is Remel Co.. The 510(k) number is K830322.

When did C.A.T. REAGENT KIT receive FDA 510(k) clearance?

C.A.T. REAGENT KIT received FDA 510(k) clearance on 1983-03-28, under 510(k) number K830322.

Who is the listed applicant for C.A.T. REAGENT KIT?

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

What is the FDA product code for C.A.T. REAGENT KIT?

The FDA product code for C.A.T. REAGENT KIT is JTQ.

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 Remel Co. 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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

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Related Devices (Code: JTQ)

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.

K875275WINTHROP PHARMACEUTICALS CONTRAST MEDIA WARMERSterling Drug, Inc.K853379PLATE INCUBATORScientific Sales Intl., Inc.K831592ANHYDRIC INCUBATORS, CULTURE INCUBATORBoekel Industries, Inc.K830227AUTOMATED ELISA READER LBI 300Bionetic Laboratory ProductsK830405LBI-100 37DEGREES INCUBATORBionetic Laboratory ProductsK822564WATER BATHBoekel Industries, Inc.

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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