Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HARRIS HEMATOXYLIN, MERCURY FREE, ACID

K-Number: K843425 · 1984-10-02

Decision Date1984-10-02
Product CodeHYK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HARRIS HEMATOXYLIN, MERCURY FREE, ACID is the device name listed in this FDA 510(k) record. The listed applicant is Accra Laboratories, Inc.. It received FDA 510(k) clearance on 1984-10-02 under 510(k) number K843425. The device is classified under product code HYK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARRIS HEMATOXYLIN, MERCURY FREE, ACID?

HARRIS HEMATOXYLIN, MERCURY FREE, ACID is a medical device that received FDA 510(k) clearance on 1984-10-02. The listed applicant is Accra Laboratories, Inc.. The 510(k) number is K843425.

When did HARRIS HEMATOXYLIN, MERCURY FREE, ACID receive FDA 510(k) clearance?

HARRIS HEMATOXYLIN, MERCURY FREE, ACID received FDA 510(k) clearance on 1984-10-02, under 510(k) number K843425.

Who is the listed applicant for HARRIS HEMATOXYLIN, MERCURY FREE, ACID?

The FDA 510(k) record lists Accra Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HARRIS HEMATOXYLIN, MERCURY FREE, ACID?

The FDA product code for HARRIS HEMATOXYLIN, MERCURY FREE, ACID is HYK.

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 Accra Laboratories, 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.

View all 20 devices →

Related Devices (Code: HYK)

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.

↑