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FDA 510(k)

DIMENSION(R) VALPROIC (VALP) ACID METHOD

K-Number: K982880 · 1998-08-25

Decision Date1998-08-25
Product CodeLEG
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

DIMENSION(R) VALPROIC (VALP) ACID METHOD is the device name listed in this FDA 510(k) record. The listed applicant is Dade Behring, Inc.. It received FDA 510(k) clearance on 1998-08-25 under 510(k) number K982880. The device is classified under product code LEG. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIMENSION(R) VALPROIC (VALP) ACID METHOD?

DIMENSION(R) VALPROIC (VALP) ACID METHOD is a medical device that received FDA 510(k) clearance on 1998-08-25. The listed applicant is Dade Behring, Inc.. The 510(k) number is K982880.

When did DIMENSION(R) VALPROIC (VALP) ACID METHOD receive FDA 510(k) clearance?

DIMENSION(R) VALPROIC (VALP) ACID METHOD received FDA 510(k) clearance on 1998-08-25, under 510(k) number K982880.

Who is the listed applicant for DIMENSION(R) VALPROIC (VALP) ACID METHOD?

The FDA 510(k) record lists Dade Behring, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIMENSION(R) VALPROIC (VALP) ACID METHOD?

The FDA product code for DIMENSION(R) VALPROIC (VALP) ACID METHOD 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 Dade Behring, 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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