RADCAL MODEL 4051 RADIONUCLIDE CALIBRA
K-Number: K841786 · 1984-07-16
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Device Summary
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
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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