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FDA 510(k)

JENNER BLOOD STAIN

K-Number: K842928 · 1984-09-11

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

Device Summary

JENNER BLOOD STAIN 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 K842928. The device is classified under product code KJX. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JENNER BLOOD STAIN?

JENNER BLOOD STAIN 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 K842928.

When did JENNER BLOOD STAIN receive FDA 510(k) clearance?

JENNER BLOOD STAIN received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842928.

Who is the listed applicant for JENNER BLOOD STAIN?

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 JENNER BLOOD STAIN?

The FDA product code for JENNER BLOOD STAIN is KJX.

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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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