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FDA 510(k)

HEMOCARD HEMOGLOBIN E

K-Number: K930070 · 1993-04-08

ApplicantIsolab, Inc.
Decision Date1993-04-08
Product CodeCKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

HEMOCARD HEMOGLOBIN E is the device name listed in this FDA 510(k) record. The listed applicant is Isolab, Inc.. It received FDA 510(k) clearance on 1993-04-08 under 510(k) number K930070. The device is classified under product code CKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOCARD HEMOGLOBIN E?

HEMOCARD HEMOGLOBIN E is a medical device that received FDA 510(k) clearance on 1993-04-08. The listed applicant is Isolab, Inc.. The 510(k) number is K930070.

When did HEMOCARD HEMOGLOBIN E receive FDA 510(k) clearance?

HEMOCARD HEMOGLOBIN E received FDA 510(k) clearance on 1993-04-08, under 510(k) number K930070.

Who is the listed applicant for HEMOCARD HEMOGLOBIN E?

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

What is the FDA product code for HEMOCARD HEMOGLOBIN E?

The FDA product code for HEMOCARD HEMOGLOBIN E is CKA.

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 Isolab, 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 44 devices →

Related Devices (Code: CKA)

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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