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FDA 510(k)

PARA-PAK CLEAN VIAL

K-Number: K792710 · 1980-01-28

ApplicantMeridian Diagnostics, Inc.
Decision Date1980-01-28
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

PARA-PAK CLEAN VIAL is the device name listed in this FDA 510(k) record. The listed applicant is Meridian Diagnostics, Inc.. It received FDA 510(k) clearance on 1980-01-28 under 510(k) number K792710. 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 PARA-PAK CLEAN VIAL?

PARA-PAK CLEAN VIAL is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Meridian Diagnostics, Inc.. The 510(k) number is K792710.

When did PARA-PAK CLEAN VIAL receive FDA 510(k) clearance?

PARA-PAK CLEAN VIAL received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792710.

Who is the listed applicant for PARA-PAK CLEAN VIAL?

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

What is the FDA product code for PARA-PAK CLEAN VIAL?

The FDA product code for PARA-PAK CLEAN VIAL is FMH.

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Other records listing Meridian Diagnostics, Inc. as applicant

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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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