DOCUMENT ENZYME LINEARITY TEST SETS
K-Number: K861506 · 1986-06-13
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Device Summary
Frequently Asked Questions
What is the DOCUMENT ENZYME LINEARITY TEST SETS?
DOCUMENT ENZYME LINEARITY TEST SETS is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is Casco Standards. The 510(k) number is K861506.
When did DOCUMENT ENZYME LINEARITY TEST SETS receive FDA 510(k) clearance?
DOCUMENT ENZYME LINEARITY TEST SETS received FDA 510(k) clearance on 1986-06-13, under 510(k) number K861506.
Who is the listed applicant for DOCUMENT ENZYME LINEARITY TEST SETS?
The FDA 510(k) record lists Casco Standards as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DOCUMENT ENZYME LINEARITY TEST SETS?
The FDA product code for DOCUMENT ENZYME LINEARITY TEST SETS is JJT.
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 Casco Standards 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: JJT)
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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