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FDA 510(k)

COULTER COUNTER MODEL ZM

K-Number: K843164 · 1984-11-13

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

Device Summary

COULTER COUNTER MODEL ZM is the device name listed in this FDA 510(k) record. The listed applicant is Coulter Electronics, Inc.. It received FDA 510(k) clearance on 1984-11-13 under 510(k) number K843164. The device is classified under product code GKL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COULTER COUNTER MODEL ZM?

COULTER COUNTER MODEL ZM is a medical device that received FDA 510(k) clearance on 1984-11-13. The listed applicant is Coulter Electronics, Inc.. The 510(k) number is K843164.

When did COULTER COUNTER MODEL ZM receive FDA 510(k) clearance?

COULTER COUNTER MODEL ZM received FDA 510(k) clearance on 1984-11-13, under 510(k) number K843164.

Who is the listed applicant for COULTER COUNTER MODEL ZM?

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

What is the FDA product code for COULTER COUNTER MODEL ZM?

The FDA product code for COULTER COUNTER MODEL ZM is GKL.

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 Coulter Electronics, 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 101 devices →

Related Devices (Code: GKL)

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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