CAFFEIC ACID DISK
K-Number: K850194 · 1985-04-22
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Device Summary
Frequently Asked Questions
What is the CAFFEIC ACID DISK?
CAFFEIC ACID DISK is a medical device that received FDA 510(k) clearance on 1985-04-22. The listed applicant is Remel Co.. The 510(k) number is K850194.
When did CAFFEIC ACID DISK receive FDA 510(k) clearance?
CAFFEIC ACID DISK received FDA 510(k) clearance on 1985-04-22, under 510(k) number K850194.
Who is the listed applicant for CAFFEIC ACID DISK?
The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CAFFEIC ACID DISK?
The FDA product code for CAFFEIC ACID DISK is JSF.
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 Remel Co. 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: JSF)
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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