CHOLESTEROL CALIBRATORS
K-Number: K861314 · 1986-07-01
Advertisement
Device Summary
Frequently Asked Questions
What is the CHOLESTEROL CALIBRATORS?
CHOLESTEROL CALIBRATORS is a medical device that received FDA 510(k) clearance on 1986-07-01. The listed applicant is Sigma Diagnostics, Inc.. The 510(k) number is K861314.
When did CHOLESTEROL CALIBRATORS receive FDA 510(k) clearance?
CHOLESTEROL CALIBRATORS received FDA 510(k) clearance on 1986-07-01, under 510(k) number K861314.
Who is the listed applicant for CHOLESTEROL CALIBRATORS?
The FDA 510(k) record lists Sigma Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHOLESTEROL CALIBRATORS?
The FDA product code for CHOLESTEROL CALIBRATORS is JIT.
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 Sigma Diagnostics, 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: JIT)
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.
Advertisement