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FDA 510(k)

CHART-TYPE MICRO HEMATOCRIT TUBE READER

K-Number: K870511 · 1987-03-16

Decision Date1987-03-16
Product CodeJPI
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CHART-TYPE MICRO HEMATOCRIT TUBE READER is the device name listed in this FDA 510(k) record. The listed applicant is Norfolk Scientific, Inc.. It received FDA 510(k) clearance on 1987-03-16 under 510(k) number K870511. The device is classified under product code JPI. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHART-TYPE MICRO HEMATOCRIT TUBE READER?

CHART-TYPE MICRO HEMATOCRIT TUBE READER is a medical device that received FDA 510(k) clearance on 1987-03-16. The listed applicant is Norfolk Scientific, Inc.. The 510(k) number is K870511.

When did CHART-TYPE MICRO HEMATOCRIT TUBE READER receive FDA 510(k) clearance?

CHART-TYPE MICRO HEMATOCRIT TUBE READER received FDA 510(k) clearance on 1987-03-16, under 510(k) number K870511.

Who is the listed applicant for CHART-TYPE MICRO HEMATOCRIT TUBE READER?

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

What is the FDA product code for CHART-TYPE MICRO HEMATOCRIT TUBE READER?

The FDA product code for CHART-TYPE MICRO HEMATOCRIT TUBE READER is JPI.

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 Norfolk Scientific, 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 7 devices →

Related Devices (Code: JPI)

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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