VOGES-PROSKAUER REAGENT A
K-Number: K842870 · 1984-08-03
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Device Summary
Frequently Asked Questions
What is the VOGES-PROSKAUER REAGENT A?
VOGES-PROSKAUER REAGENT A is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Irvine Diagnostic Services. The 510(k) number is K842870.
When did VOGES-PROSKAUER REAGENT A receive FDA 510(k) clearance?
VOGES-PROSKAUER REAGENT A received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842870.
Who is the listed applicant for VOGES-PROSKAUER REAGENT A?
The FDA 510(k) record lists Irvine Diagnostic Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOGES-PROSKAUER REAGENT A?
The FDA product code for VOGES-PROSKAUER REAGENT A 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 Irvine Diagnostic Services 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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