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FDA 510(k)

ABCO MIDSTREAM URINE COLLECTION SET

K-Number: K800233 · 1980-02-26

ApplicantAbco Dealers, Inc.
Decision Date1980-02-26
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

ABCO MIDSTREAM URINE COLLECTION SET 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 1980-02-26 under 510(k) number K800233. The device is classified under product code FMH. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABCO MIDSTREAM URINE COLLECTION SET?

ABCO MIDSTREAM URINE COLLECTION SET is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K800233.

When did ABCO MIDSTREAM URINE COLLECTION SET receive FDA 510(k) clearance?

ABCO MIDSTREAM URINE COLLECTION SET received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800233.

Who is the listed applicant for ABCO MIDSTREAM URINE COLLECTION SET?

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 ABCO MIDSTREAM URINE COLLECTION SET?

The FDA product code for ABCO MIDSTREAM URINE COLLECTION SET is FMH.

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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.

K905025DIGITAL THERMOMETER KITSK882304DIGITAL THERMOMETER SHEATHS (ORAL AND RECTAL)K880892BLOOD COLLECTING NEEDLE AND HOLDERSK880894ALLERGIST SYRINGESK872875STRETCH GAUZE BANDAGESK872874MICROSCOPE COVER GLASSES

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Related Devices (Code: FMH)

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.

K900983TRI-TECH URINE SPECIMEN KITTri-Tech, Inc.K823763VARIOUS-SPECIMEN COLLECTORSCordis Corp.K820180CALCULI FILTER CUPOmnimedicalK812933LANCER SPECIMEN CONTAINERSherwood Medical Co.K802340SPECIMEN SETAmerican Pharmaseal Div. AhscK802002URINE SPECIMEN CONTAINER #'S 1013-1016Pollak (Intl.), Ltd.

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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