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FDA 510(k)

COLE TUBE-LATEX

K-Number: K840973 · 1984-03-30

ApplicantInmed Corp.
Decision Date1984-03-30
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

COLE TUBE-LATEX is the device name listed in this FDA 510(k) record. The listed applicant is Inmed Corp.. It received FDA 510(k) clearance on 1984-03-30 under 510(k) number K840973. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLE TUBE-LATEX?

COLE TUBE-LATEX is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Inmed Corp.. The 510(k) number is K840973.

When did COLE TUBE-LATEX receive FDA 510(k) clearance?

COLE TUBE-LATEX received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840973.

Who is the listed applicant for COLE TUBE-LATEX?

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

What is the FDA product code for COLE TUBE-LATEX?

The FDA product code for COLE TUBE-LATEX is BTR.

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Related Devices (Code: BTR)

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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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