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FDA 510(k)

MID-STREAM COLLECTION SET

K-Number: K770231 · 1977-03-30

ApplicantChesire Laboratories
Decision Date1977-03-30
Product CodeFMH
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MID-STREAM COLLECTION SET is the device name listed in this FDA 510(k) record. The listed applicant is Chesire Laboratories. It received FDA 510(k) clearance on 1977-03-30 under 510(k) number K770231. 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 MID-STREAM COLLECTION SET?

MID-STREAM COLLECTION SET is a medical device that received FDA 510(k) clearance on 1977-03-30. The listed applicant is Chesire Laboratories. The 510(k) number is K770231.

When did MID-STREAM COLLECTION SET receive FDA 510(k) clearance?

MID-STREAM COLLECTION SET received FDA 510(k) clearance on 1977-03-30, under 510(k) number K770231.

Who is the listed applicant for MID-STREAM COLLECTION SET?

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

What is the FDA product code for MID-STREAM COLLECTION SET?

The FDA product code for MID-STREAM COLLECTION SET is FMH.

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Other records listing Chesire Laboratories 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.

K924265DOCTOR'S CHOICE LATEX EXAMINATION GLOVESK924266DOCTOR'S CHOICE POWDER FREE LATEX EXAM GLOVESK770233STERILE SUCTION CATHETER W/CONTROL

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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