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FDA 510(k)

BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK

K-Number: K770076 · 1977-03-22

Decision Date1977-03-22
Product CodeKPA
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK is the device name listed in this FDA 510(k) record. The listed applicant is Jack W. Kindberg. It received FDA 510(k) clearance on 1977-03-22 under 510(k) number K770076. The device is classified under product code KPA. It was reviewed by the PA advisory panel. Product code KPA falls under the category of Cardiovascular, which encompasses devices for cardiovascular diagnosis, monitoring, and intervention. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK?

BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK is a medical device that received FDA 510(k) clearance on 1977-03-22. The listed applicant is Jack W. Kindberg. The 510(k) number is K770076.

When did BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK receive FDA 510(k) clearance?

BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK received FDA 510(k) clearance on 1977-03-22, under 510(k) number K770076.

Who is the listed applicant for BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK?

The FDA 510(k) record lists Jack W. Kindberg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK?

The FDA product code for BIO-DYES FORT. WRIGHTS STAIN HEMAT. PACK is KPA. This falls under the Cardiovascular category.

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 Jack W. Kindberg 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.

Related Devices (Code: KPA)

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

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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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