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FDA 510(k)

LIGHT GREEN SF 1%

K-Number: K842927 · 1984-09-11

ApplicantE K Ind., Inc.
Decision Date1984-09-11
Product CodeHYS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

LIGHT GREEN SF 1% 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 1984-09-11 under 510(k) number K842927. The device is classified under product code HYS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT GREEN SF 1%?

LIGHT GREEN SF 1% is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is E K Ind., Inc.. The 510(k) number is K842927.

When did LIGHT GREEN SF 1% receive FDA 510(k) clearance?

LIGHT GREEN SF 1% received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842927.

Who is the listed applicant for LIGHT GREEN SF 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 LIGHT GREEN SF 1%?

The FDA product code for LIGHT GREEN SF 1% is HYS.

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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.

K842931DRABKIN REAGENTK842938ACETIC ACID 1% V/VK842934DECOLORIZING FLUIC, ACID-ALCOHOL 3%K842937ACETIC ACID 2% V/VK842935ACETIC ACID, 5% V/VK842936ACETIC ACID, 3% V/V

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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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