CHOLESTEROL RAPID SLAT KIT HDL
K-Number: K780331 · 1978-04-06
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Device Summary
Frequently Asked Questions
What is the CHOLESTEROL RAPID SLAT KIT HDL?
CHOLESTEROL RAPID SLAT KIT HDL is a medical device that received FDA 510(k) clearance on 1978-04-06. The listed applicant is Pierce Chemical Co.. The 510(k) number is K780331.
When did CHOLESTEROL RAPID SLAT KIT HDL receive FDA 510(k) clearance?
CHOLESTEROL RAPID SLAT KIT HDL received FDA 510(k) clearance on 1978-04-06, under 510(k) number K780331.
Who is the listed applicant for CHOLESTEROL RAPID SLAT KIT HDL?
The FDA 510(k) record lists Pierce Chemical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHOLESTEROL RAPID SLAT KIT HDL?
The FDA product code for CHOLESTEROL RAPID SLAT KIT HDL 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 Pierce Chemical Co. 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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