SAFRANIN, 1% W/V
K-Number: K842920 · 1984-07-25
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Device Summary
Frequently Asked Questions
What is the SAFRANIN, 1% W/V?
SAFRANIN, 1% W/V is a medical device that received FDA 510(k) clearance on 1984-07-25. The listed applicant is E K Ind., Inc.. The 510(k) number is K842920.
When did SAFRANIN, 1% W/V receive FDA 510(k) clearance?
SAFRANIN, 1% W/V received FDA 510(k) clearance on 1984-07-25, under 510(k) number K842920.
Who is the listed applicant for SAFRANIN, 1% W/V?
The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
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 E K Ind., 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.
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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