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FDA 510(k)

ACETIC ACID 1% V/V

K-Number: K842938 · 1984-09-14

ApplicantE K Ind., Inc.
Decision Date1984-09-14
Product CodeGGK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

ACETIC ACID 1% V/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 1984-09-14 under 510(k) number K842938. The device is classified under product code GGK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETIC ACID 1% V/V?

ACETIC ACID 1% V/V is a medical device that received FDA 510(k) clearance on 1984-09-14. The listed applicant is E K Ind., Inc.. The 510(k) number is K842938.

When did ACETIC ACID 1% V/V receive FDA 510(k) clearance?

ACETIC ACID 1% V/V received FDA 510(k) clearance on 1984-09-14, under 510(k) number K842938.

Who is the listed applicant for ACETIC ACID 1% V/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 ACETIC ACID 1% V/V?

The FDA product code for ACETIC ACID 1% V/V is GGK.

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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 REAGENTK842936ACETIC ACID, 3% V/VK842937ACETIC ACID 2% V/VK842934DECOLORIZING FLUIC, ACID-ALCOHOL 3%K842935ACETIC ACID, 5% V/VK842739PAP STAIN, EA-36

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Related Devices (Code: GGK)

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.

K883836COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-IICoulter ImmunologyK883991KVM HEMOGLOBIN LYSING REAGENTKvm Technologies, Inc.K874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENTFisher Scientific Co., LLCK873348CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.Abbott DiagnosticsK863114PIASTRINITJ. D. Assoc.K863503HEMOLYSEReagent Laboratory, Inc.

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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