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FDA 510(k)

DATES-OHMEDA AESTIVA SMARTVENT MRI

K-Number: K993410 · 2000-04-25

ApplicantDatex-Ohmeda, Inc.
Decision Date2000-04-25
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DATES-OHMEDA AESTIVA SMARTVENT MRI is the device name listed in this FDA 510(k) record. The listed applicant is Datex-Ohmeda, Inc.. It received FDA 510(k) clearance on 2000-04-25 under 510(k) number K993410. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DATES-OHMEDA AESTIVA SMARTVENT MRI?

DATES-OHMEDA AESTIVA SMARTVENT MRI is a medical device that received FDA 510(k) clearance on 2000-04-25. The listed applicant is Datex-Ohmeda, Inc.. The 510(k) number is K993410.

When did DATES-OHMEDA AESTIVA SMARTVENT MRI receive FDA 510(k) clearance?

DATES-OHMEDA AESTIVA SMARTVENT MRI received FDA 510(k) clearance on 2000-04-25, under 510(k) number K993410.

Who is the listed applicant for DATES-OHMEDA AESTIVA SMARTVENT MRI?

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

What is the FDA product code for DATES-OHMEDA AESTIVA SMARTVENT MRI?

The FDA product code for DATES-OHMEDA AESTIVA SMARTVENT MRI is BSZ.

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Related Devices (Code: BSZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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