VMA BY HPLC TEST (VANILMANDELIC ACID)
K-Number: K861010 · 1986-05-01
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Device Summary
Frequently Asked Questions
What is the VMA BY HPLC TEST (VANILMANDELIC ACID)?
VMA BY HPLC TEST (VANILMANDELIC ACID) is a medical device that received FDA 510(k) clearance on 1986-05-01. The listed applicant is Bio-Rad. The 510(k) number is K861010.
When did VMA BY HPLC TEST (VANILMANDELIC ACID) receive FDA 510(k) clearance?
VMA BY HPLC TEST (VANILMANDELIC ACID) received FDA 510(k) clearance on 1986-05-01, under 510(k) number K861010.
Who is the listed applicant for VMA BY HPLC TEST (VANILMANDELIC ACID)?
The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VMA BY HPLC TEST (VANILMANDELIC ACID)?
The FDA product code for VMA BY HPLC TEST (VANILMANDELIC ACID) is CDF.
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 Bio-Rad 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: CDF)
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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