VALPROIC ACID
K-Number: K936208 · 1994-03-11
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Device Summary
Frequently Asked Questions
What is the VALPROIC ACID?
VALPROIC ACID is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Seradyn, Inc.. The 510(k) number is K936208.
When did VALPROIC ACID receive FDA 510(k) clearance?
VALPROIC ACID received FDA 510(k) clearance on 1994-03-11, under 510(k) number K936208.
Who is the listed applicant for VALPROIC ACID?
The FDA 510(k) record lists Seradyn, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VALPROIC ACID?
The FDA product code for VALPROIC ACID is LEG.
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 Seradyn, 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.
Related Devices (Code: LEG)
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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