HORMONE KIT, PARATHYROID
K-Number: K782010 · 1979-01-10
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Device Summary
Frequently Asked Questions
What is the HORMONE KIT, PARATHYROID?
HORMONE KIT, PARATHYROID is a medical device that received FDA 510(k) clearance on 1979-01-10. The listed applicant is Nichols Institute Diagnostics. The 510(k) number is K782010.
When did HORMONE KIT, PARATHYROID receive FDA 510(k) clearance?
HORMONE KIT, PARATHYROID received FDA 510(k) clearance on 1979-01-10, under 510(k) number K782010.
Who is the listed applicant for HORMONE KIT, PARATHYROID?
The FDA 510(k) record lists Nichols Institute Diagnostics as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HORMONE KIT, PARATHYROID?
The FDA product code for HORMONE KIT, PARATHYROID is CEW.
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 Nichols Institute Diagnostics 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: CEW)
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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