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FDA 510(k)

MVP-10 MRI INFANT VENTILATOR

K-Number: K896381 · 1990-02-12

Decision Date1990-02-12
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MVP-10 MRI INFANT VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Med Devices, Inc.. It received FDA 510(k) clearance on 1990-02-12 under 510(k) number K896381. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MVP-10 MRI INFANT VENTILATOR?

MVP-10 MRI INFANT VENTILATOR is a medical device that received FDA 510(k) clearance on 1990-02-12. The listed applicant is Bio-Med Devices, Inc.. The 510(k) number is K896381.

When did MVP-10 MRI INFANT VENTILATOR receive FDA 510(k) clearance?

MVP-10 MRI INFANT VENTILATOR received FDA 510(k) clearance on 1990-02-12, under 510(k) number K896381.

Who is the listed applicant for MVP-10 MRI INFANT VENTILATOR?

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

What is the FDA product code for MVP-10 MRI INFANT VENTILATOR?

The FDA product code for MVP-10 MRI INFANT VENTILATOR is CBK.

Related Clinical Trials

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.

Other records listing Bio-Med Devices, Inc. as applicant

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.

View all 14 devices →

Related Devices (Code: CBK)

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.

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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