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FDA 510(k)

MICRO HEMATOCRIT CAPILLARY TUBES

K-Number: K843892 · 1984-11-13

Decision Date1984-11-13
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

MICRO HEMATOCRIT CAPILLARY TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1984-11-13 under 510(k) number K843892. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO HEMATOCRIT CAPILLARY TUBES?

MICRO HEMATOCRIT CAPILLARY TUBES is a medical device that received FDA 510(k) clearance on 1984-11-13. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K843892.

When did MICRO HEMATOCRIT CAPILLARY TUBES receive FDA 510(k) clearance?

MICRO HEMATOCRIT CAPILLARY TUBES received FDA 510(k) clearance on 1984-11-13, under 510(k) number K843892.

Who is the listed applicant for MICRO HEMATOCRIT CAPILLARY TUBES?

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

What is the FDA product code for MICRO HEMATOCRIT CAPILLARY TUBES?

The FDA product code for MICRO HEMATOCRIT CAPILLARY TUBES is GIO.

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 Abco Dealers, 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 127 devices →

Related Devices (Code: GIO)

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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