PDA CHOLESTEROL
K-Number: K843510 · 1984-09-28
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Device Summary
Frequently Asked Questions
What is the PDA CHOLESTEROL?
PDA CHOLESTEROL is a medical device that received FDA 510(k) clearance on 1984-09-28. The listed applicant is Abbott Laboratories. The 510(k) number is K843510.
When did PDA CHOLESTEROL receive FDA 510(k) clearance?
PDA CHOLESTEROL received FDA 510(k) clearance on 1984-09-28, under 510(k) number K843510.
Who is the listed applicant for PDA CHOLESTEROL?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PDA CHOLESTEROL?
The FDA product code for PDA CHOLESTEROL is CHH.
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 Abbott Laboratories 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: CHH)
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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