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FDA 510(k)

TRIGLYCERIDE (TRINDER) PROCEDURE

K-Number: K861670 · 1986-07-01

Decision Date1986-07-01
Product CodeCDT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TRIGLYCERIDE (TRINDER) PROCEDURE is the device name listed in this FDA 510(k) record. The listed applicant is Data Medical Associates, Inc.. It received FDA 510(k) clearance on 1986-07-01 under 510(k) number K861670. The device is classified under product code CDT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIGLYCERIDE (TRINDER) PROCEDURE?

TRIGLYCERIDE (TRINDER) PROCEDURE is a medical device that received FDA 510(k) clearance on 1986-07-01. The listed applicant is Data Medical Associates, Inc.. The 510(k) number is K861670.

When did TRIGLYCERIDE (TRINDER) PROCEDURE receive FDA 510(k) clearance?

TRIGLYCERIDE (TRINDER) PROCEDURE received FDA 510(k) clearance on 1986-07-01, under 510(k) number K861670.

Who is the listed applicant for TRIGLYCERIDE (TRINDER) PROCEDURE?

The FDA 510(k) record lists Data Medical Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIGLYCERIDE (TRINDER) PROCEDURE?

The FDA product code for TRIGLYCERIDE (TRINDER) PROCEDURE is CDT.

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 Data Medical Associates, 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.

View all 111 devices →

Related Devices (Code: CDT)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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