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FDA 510(k)

MEDRAD ATD-T INTERFACE DEVICE

K-Number: K974438 · 1998-04-30

ApplicantMedrad, Inc.
Decision Date1998-04-30
Product CodeMOS
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDRAD ATD-T INTERFACE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1998-04-30 under 510(k) number K974438. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDRAD ATD-T INTERFACE DEVICE?

MEDRAD ATD-T INTERFACE DEVICE is a medical device that received FDA 510(k) clearance on 1998-04-30. The listed applicant is Medrad, Inc.. The 510(k) number is K974438.

When did MEDRAD ATD-T INTERFACE DEVICE receive FDA 510(k) clearance?

MEDRAD ATD-T INTERFACE DEVICE received FDA 510(k) clearance on 1998-04-30, under 510(k) number K974438.

Who is the listed applicant for MEDRAD ATD-T INTERFACE DEVICE?

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

What is the FDA product code for MEDRAD ATD-T INTERFACE DEVICE?

The FDA product code for MEDRAD ATD-T INTERFACE DEVICE is MOS.

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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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