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FDA 510(k)

MICROTEK MEDICAL'S BLOOD COLLECTION KIT

K-Number: K900726 · 1990-05-04

Decision Date1990-05-04
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MICROTEK MEDICAL'S BLOOD COLLECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Microbio-Medics, Inc.. It received FDA 510(k) clearance on 1990-05-04 under 510(k) number K900726. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROTEK MEDICAL'S BLOOD COLLECTION KIT?

MICROTEK MEDICAL'S BLOOD COLLECTION KIT is a medical device that received FDA 510(k) clearance on 1990-05-04. The listed applicant is Microbio-Medics, Inc.. The 510(k) number is K900726.

When did MICROTEK MEDICAL'S BLOOD COLLECTION KIT receive FDA 510(k) clearance?

MICROTEK MEDICAL'S BLOOD COLLECTION KIT received FDA 510(k) clearance on 1990-05-04, under 510(k) number K900726.

Who is the listed applicant for MICROTEK MEDICAL'S BLOOD COLLECTION KIT?

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

What is the FDA product code for MICROTEK MEDICAL'S BLOOD COLLECTION KIT?

The FDA product code for MICROTEK MEDICAL'S BLOOD COLLECTION KIT is JKA.

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 Microbio-Medics, 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 13 devices →

Related Devices (Code: JKA)

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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