ORANGE G, 1%
K-Number: K842924 · 1984-09-07
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Device Summary
Frequently Asked Questions
What is the ORANGE G, 1%?
ORANGE G, 1% is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is E K Ind., Inc.. The 510(k) number is K842924.
When did ORANGE G, 1% receive FDA 510(k) clearance?
ORANGE G, 1% received FDA 510(k) clearance on 1984-09-07, under 510(k) number K842924.
Who is the listed applicant for ORANGE G, 1%?
The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ORANGE G, 1%?
The FDA product code for ORANGE G, 1% is HZH.
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.
Related Devices (Code: HZH)
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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