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FDA 510(k)

FOCUS FLUID

K-Number: K830187 · 1983-03-01

ApplicantHematology Marketing Assoc.
Decision Date1983-03-01
Product CodeEIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FOCUS FLUID is the device name listed in this FDA 510(k) record. The listed applicant is Hematology Marketing Assoc.. It received FDA 510(k) clearance on 1983-03-01 under 510(k) number K830187. The device is classified under product code EIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOCUS FLUID?

FOCUS FLUID is a medical device that received FDA 510(k) clearance on 1983-03-01. The listed applicant is Hematology Marketing Assoc.. The 510(k) number is K830187.

When did FOCUS FLUID receive FDA 510(k) clearance?

FOCUS FLUID received FDA 510(k) clearance on 1983-03-01, under 510(k) number K830187.

Who is the listed applicant for FOCUS FLUID?

The FDA 510(k) record lists Hematology Marketing Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FOCUS FLUID?

The FDA product code for FOCUS FLUID is EIF.

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Other records listing Hematology Marketing Assoc. 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.

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Related Devices (Code: EIF)

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.

K940785MOUTH PROPSWorldwide Dental, Inc.K873960LEWIS SAFE SLEEVECheri Lewis, D.D.S.K830116SULCARINGSNorth Pacific Dental, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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