RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL
K-Number: K871508 · 1987-05-08
Advertisement
Device Summary
Frequently Asked Questions
What is the RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL?
RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL is a medical device that received FDA 510(k) clearance on 1987-05-08. The listed applicant is Trace Scientific , Ltd.. The 510(k) number is K871508.
When did RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL receive FDA 510(k) clearance?
RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL received FDA 510(k) clearance on 1987-05-08, under 510(k) number K871508.
Who is the listed applicant for RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL?
The FDA 510(k) record lists Trace Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL?
The FDA product code for RESUBMITTED TRIGLYCERIDE GPO - TWO VIAL 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 Trace Scientific , Ltd. 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: 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement