PERIDOCHROM TRIGLYCERIDES GPO
K-Number: K850667 · 1985-03-11
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Device Summary
Frequently Asked Questions
What is the PERIDOCHROM TRIGLYCERIDES GPO?
PERIDOCHROM TRIGLYCERIDES GPO is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K850667.
When did PERIDOCHROM TRIGLYCERIDES GPO receive FDA 510(k) clearance?
PERIDOCHROM TRIGLYCERIDES GPO received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850667.
Who is the listed applicant for PERIDOCHROM TRIGLYCERIDES GPO?
The FDA 510(k) record lists Boehringer Mannheim Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERIDOCHROM TRIGLYCERIDES GPO?
The FDA product code for PERIDOCHROM TRIGLYCERIDES GPO 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 Boehringer Mannheim Corp. 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.
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