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FDA 510(k)

RADCAL MODEL 4051 RADIONUCLIDE CALIBRA

K-Number: K841786 · 1984-07-16

ApplicantRadcal Corp.
Decision Date1984-07-16
Product CodeKPT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

RADCAL MODEL 4051 RADIONUCLIDE CALIBRA is the device name listed in this FDA 510(k) record. The listed applicant is Radcal Corp.. It received FDA 510(k) clearance on 1984-07-16 under 510(k) number K841786. The device is classified under product code KPT. It was reviewed by the RA advisory panel. Product code KPT falls under the category of In Vitro Diagnostics, which includes laboratory reagents and diagnostic test kits. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADCAL MODEL 4051 RADIONUCLIDE CALIBRA?

RADCAL MODEL 4051 RADIONUCLIDE CALIBRA is a medical device that received FDA 510(k) clearance on 1984-07-16. The listed applicant is Radcal Corp.. The 510(k) number is K841786.

When did RADCAL MODEL 4051 RADIONUCLIDE CALIBRA receive FDA 510(k) clearance?

RADCAL MODEL 4051 RADIONUCLIDE CALIBRA received FDA 510(k) clearance on 1984-07-16, under 510(k) number K841786.

Who is the listed applicant for RADCAL MODEL 4051 RADIONUCLIDE CALIBRA?

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

What is the FDA product code for RADCAL MODEL 4051 RADIONUCLIDE CALIBRA?

The FDA product code for RADCAL MODEL 4051 RADIONUCLIDE CALIBRA is KPT. This falls under the In Vitro Diagnostics category.

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 Radcal 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.

Related Devices (Code: KPT)

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

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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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