SULFOSALICYLIC ACID, 3% W/V
K-Number: K842915 · 1984-08-10
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Device Summary
Frequently Asked Questions
What is the SULFOSALICYLIC ACID, 3% W/V?
SULFOSALICYLIC ACID, 3% W/V is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is E K Ind., Inc.. The 510(k) number is K842915.
When did SULFOSALICYLIC ACID, 3% W/V receive FDA 510(k) clearance?
SULFOSALICYLIC ACID, 3% W/V received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842915.
Who is the listed applicant for SULFOSALICYLIC ACID, 3% W/V?
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 SULFOSALICYLIC ACID, 3% W/V?
The FDA product code for SULFOSALICYLIC ACID, 3% W/V is JIQ.
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: JIQ)
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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