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FDA 510(k)

SPECIMEN COLLECTION PAN

K-Number: K800309 · 1980-02-26

ApplicantSage Products, Inc.
Decision Date1980-02-26
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

SPECIMEN COLLECTION PAN is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1980-02-26 under 510(k) number K800309. 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 SPECIMEN COLLECTION PAN?

SPECIMEN COLLECTION PAN is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Sage Products, Inc.. The 510(k) number is K800309.

When did SPECIMEN COLLECTION PAN receive FDA 510(k) clearance?

SPECIMEN COLLECTION PAN received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800309.

Who is the listed applicant for SPECIMEN COLLECTION PAN?

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

What is the FDA product code for SPECIMEN COLLECTION PAN?

The FDA product code for SPECIMEN COLLECTION PAN is FMH.

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Other records listing Sage Products, 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.

K972705RESHEATHER DEVICE-METAL OR PLASTIC, RESHEATER/ NEEDLE HOLDER DEVICE-PLASTICK980490SAGE PRODUCTS INC, SHARPS DISPOSAL CONTAINERS WITH SCREW TOP CAPSK9739112 GALLON ALTERNATE CARE SHARPS CONTAINERK972279SHARPS SHUTTLEK970135NITRILE GLOVESK972302POCKET COUNT OR SAFETCOUNT

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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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