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FDA 510(k)

SAFRANIN, 1% W/V

K-Number: K842920 · 1984-07-25

Decision Date1984-07-25
Product Code
DecisionUnknown

Device Summary

SAFRANIN, 1% W/V is the device name listed in this FDA 510(k) record. The listed applicant is E K Ind., Inc.. It received FDA 510(k) clearance on 1984-07-25 under 510(k) number K842920. FDA Decision: Unknown.

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.

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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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