PRECIMAT GLYCEROL
K-Number: K780439 · 1978-04-18
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Device Summary
Frequently Asked Questions
What is the PRECIMAT GLYCEROL?
PRECIMAT GLYCEROL is a medical device that received FDA 510(k) clearance on 1978-04-18. The listed applicant is Boehringer Mannheim Corp.. The 510(k) number is K780439.
When did PRECIMAT GLYCEROL receive FDA 510(k) clearance?
PRECIMAT GLYCEROL received FDA 510(k) clearance on 1978-04-18, under 510(k) number K780439.
Who is the listed applicant for PRECIMAT GLYCEROL?
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 PRECIMAT GLYCEROL?
The FDA product code for PRECIMAT GLYCEROL is JGW.
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: JGW)
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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