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FDA 510(k)

AUTONEB ACCESSORY CROSS (AAC)

K-Number: K944643 · 1994-10-04

ApplicantVortran Medical Technology 1, Inc.
Decision Date1994-10-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTONEB ACCESSORY CROSS (AAC) is the device name listed in this FDA 510(k) record. The listed applicant is Vortran Medical Technology 1, Inc.. It received FDA 510(k) clearance on 1994-10-04 under 510(k) number K944643. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTONEB ACCESSORY CROSS (AAC)?

AUTONEB ACCESSORY CROSS (AAC) is a medical device that received FDA 510(k) clearance on 1994-10-04. The listed applicant is Vortran Medical Technology 1, Inc.. The 510(k) number is K944643.

When did AUTONEB ACCESSORY CROSS (AAC) receive FDA 510(k) clearance?

AUTONEB ACCESSORY CROSS (AAC) received FDA 510(k) clearance on 1994-10-04, under 510(k) number K944643.

Who is the listed applicant for AUTONEB ACCESSORY CROSS (AAC)?

The FDA 510(k) record lists Vortran Medical Technology 1, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUTONEB ACCESSORY CROSS (AAC)?

The FDA product code for AUTONEB ACCESSORY CROSS (AAC) is CAF.

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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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