CALCITONIN RIA KIT
K-Number: K872880 · 1987-08-13
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Device Summary
Frequently Asked Questions
What is the CALCITONIN RIA KIT?
CALCITONIN RIA KIT is a medical device that received FDA 510(k) clearance on 1987-08-13. The listed applicant is Endocrine Associates, Inc.. The 510(k) number is K872880.
When did CALCITONIN RIA KIT receive FDA 510(k) clearance?
CALCITONIN RIA KIT received FDA 510(k) clearance on 1987-08-13, under 510(k) number K872880.
Who is the listed applicant for CALCITONIN RIA KIT?
The FDA 510(k) record lists Endocrine Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CALCITONIN RIA KIT?
The FDA product code for CALCITONIN RIA KIT is JKR.
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 Endocrine Associates, Inc. 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: JKR)
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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