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FDA 510(k)

CONTINUOUS VOLUME VENTILATOR MODEL LP10

K-Number: K903010 · 1990-11-30

Decision Date1990-11-30
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS VOLUME VENTILATOR MODEL LP10 is the device name listed in this FDA 510(k) record. The listed applicant is Aequitron Medical, Inc.. It received FDA 510(k) clearance on 1990-11-30 under 510(k) number K903010. 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 CONTINUOUS VOLUME VENTILATOR MODEL LP10?

CONTINUOUS VOLUME VENTILATOR MODEL LP10 is a medical device that received FDA 510(k) clearance on 1990-11-30. The listed applicant is Aequitron Medical, Inc.. The 510(k) number is K903010.

When did CONTINUOUS VOLUME VENTILATOR MODEL LP10 receive FDA 510(k) clearance?

CONTINUOUS VOLUME VENTILATOR MODEL LP10 received FDA 510(k) clearance on 1990-11-30, under 510(k) number K903010.

Who is the listed applicant for CONTINUOUS VOLUME VENTILATOR MODEL LP10?

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

What is the FDA product code for CONTINUOUS VOLUME VENTILATOR MODEL LP10?

The FDA product code for CONTINUOUS VOLUME VENTILATOR MODEL LP10 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 Aequitron Medical, 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 24 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

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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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