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FDA 510(k)

PAPINCOLABU STAIN EA-36/50/65 & OG-6

K-Number: K823329 · 1982-12-28

Decision Date1982-12-28
Product CodeHZL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PAPINCOLABU STAIN EA-36/50/65 & OG-6 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 1982-12-28 under 510(k) number K823329. The device is classified under product code HZL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAPINCOLABU STAIN EA-36/50/65 & OG-6?

PAPINCOLABU STAIN EA-36/50/65 & OG-6 is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Accra Laboratories, Inc.. The 510(k) number is K823329.

When did PAPINCOLABU STAIN EA-36/50/65 & OG-6 receive FDA 510(k) clearance?

PAPINCOLABU STAIN EA-36/50/65 & OG-6 received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823329.

Who is the listed applicant for PAPINCOLABU STAIN EA-36/50/65 & OG-6?

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 PAPINCOLABU STAIN EA-36/50/65 & OG-6?

The FDA product code for PAPINCOLABU STAIN EA-36/50/65 & OG-6 is HZL.

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.

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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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