DPC GASTRIN KIT
K-Number: K833489 · 1984-01-30
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Device Summary
Frequently Asked Questions
What is the DPC GASTRIN KIT?
DPC GASTRIN KIT is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Diagnostic Products Corp.. The 510(k) number is K833489.
When did DPC GASTRIN KIT receive FDA 510(k) clearance?
DPC GASTRIN KIT received FDA 510(k) clearance on 1984-01-30, under 510(k) number K833489.
Who is the listed applicant for DPC GASTRIN KIT?
The FDA 510(k) record lists Diagnostic Products Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DPC GASTRIN KIT?
The FDA product code for DPC GASTRIN KIT is CGC.
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 Diagnostic Products 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: CGC)
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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