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FDA 510(k)

AUTOVENT MODEL 4000

K-Number: K070120 · 2007-05-03

ApplicantAllied Healthcare Products, Inc.
Decision Date2007-05-03
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOVENT MODEL 4000 is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 2007-05-03 under 510(k) number K070120. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOVENT MODEL 4000?

AUTOVENT MODEL 4000 is a medical device that received FDA 510(k) clearance on 2007-05-03. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K070120.

When did AUTOVENT MODEL 4000 receive FDA 510(k) clearance?

AUTOVENT MODEL 4000 received FDA 510(k) clearance on 2007-05-03, under 510(k) number K070120.

Who is the listed applicant for AUTOVENT MODEL 4000?

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

What is the FDA product code for AUTOVENT MODEL 4000?

The FDA product code for AUTOVENT MODEL 4000 is BTL.

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Other records listing Allied Healthcare Products, Inc. as applicant

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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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