FDA 510(k)

DOUBLE ENDED VENTED TRANSFER DEVICE

K-Number: K801108 · 1980-05-30

Decision Date1980-05-30

Product CodeFMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DOUBLE ENDED VENTED TRANSFER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Burron Medical Products, Inc.. It received FDA 510(k) clearance on 1980-05-30 under 510(k) number K801108. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOUBLE ENDED VENTED TRANSFER DEVICE?

DOUBLE ENDED VENTED TRANSFER DEVICE is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is Burron Medical Products, Inc.. The 510(k) number is K801108.

When did DOUBLE ENDED VENTED TRANSFER DEVICE receive FDA 510(k) clearance?

DOUBLE ENDED VENTED TRANSFER DEVICE received FDA 510(k) clearance on 1980-05-30, under 510(k) number K801108.

Who is the listed applicant for DOUBLE ENDED VENTED TRANSFER DEVICE?

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

What is the FDA product code for DOUBLE ENDED VENTED TRANSFER DEVICE?

The FDA product code for DOUBLE ENDED VENTED TRANSFER DEVICE is FMI.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.