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FDA 510(k)

URINOSCOPY FUNNEL

K-Number: K871671 · 1987-05-20

ApplicantPortable Medical Laboratories, Inc.
Decision Date1987-05-20
Product CodeGHO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

URINOSCOPY FUNNEL is the device name listed in this FDA 510(k) record. The listed applicant is Portable Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1987-05-20 under 510(k) number K871671. The device is classified under product code GHO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINOSCOPY FUNNEL?

URINOSCOPY FUNNEL is a medical device that received FDA 510(k) clearance on 1987-05-20. The listed applicant is Portable Medical Laboratories, Inc.. The 510(k) number is K871671.

When did URINOSCOPY FUNNEL receive FDA 510(k) clearance?

URINOSCOPY FUNNEL received FDA 510(k) clearance on 1987-05-20, under 510(k) number K871671.

Who is the listed applicant for URINOSCOPY FUNNEL?

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

What is the FDA product code for URINOSCOPY FUNNEL?

The FDA product code for URINOSCOPY FUNNEL is GHO.

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Other records listing Portable Medical Laboratories, 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.

K882101HEMOGLOBIN SCREENING DEVICEK874190CELL COUNTING GRID GRATICULEK864049MCARTHUR MICROSCOPE, STANDARD METAL VERSIONK854735MCARTHUR MICROSCOPE PLASTIC VERSION WITH ACC.K844476PORTABLE DIAGNOSTIC LABORATORYK844475SPECIMEN COLLECTION & TRANSPORT SYSTEM

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Related Devices (Code: GHO)

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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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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