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FDA 510(k)

VENTIPRESS 24 AND 14 PRESSURE VENTILATOR

K-Number: K893950 · 1989-08-03

ApplicantVentipress OY
Decision Date1989-08-03
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VENTIPRESS 24 AND 14 PRESSURE VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ventipress OY. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K893950. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTIPRESS 24 AND 14 PRESSURE VENTILATOR?

VENTIPRESS 24 AND 14 PRESSURE VENTILATOR is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Ventipress OY. The 510(k) number is K893950.

When did VENTIPRESS 24 AND 14 PRESSURE VENTILATOR receive FDA 510(k) clearance?

VENTIPRESS 24 AND 14 PRESSURE VENTILATOR received FDA 510(k) clearance on 1989-08-03, under 510(k) number K893950.

Who is the listed applicant for VENTIPRESS 24 AND 14 PRESSURE VENTILATOR?

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

What is the FDA product code for VENTIPRESS 24 AND 14 PRESSURE VENTILATOR?

The FDA product code for VENTIPRESS 24 AND 14 PRESSURE VENTILATOR is IRP.

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Related Devices (Code: IRP)

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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.

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