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FDA 510(k)

CAM-10 PVV PORTABLE VOLUME VENTILATOR

K-Number: K791033 · 1979-07-03

Decision Date1979-07-03
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAM-10 PVV PORTABLE VOLUME VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare Services, Inc.. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K791033. 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 CAM-10 PVV PORTABLE VOLUME VENTILATOR?

CAM-10 PVV PORTABLE VOLUME VENTILATOR is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Lifecare Services, Inc.. The 510(k) number is K791033.

When did CAM-10 PVV PORTABLE VOLUME VENTILATOR receive FDA 510(k) clearance?

CAM-10 PVV PORTABLE VOLUME VENTILATOR received FDA 510(k) clearance on 1979-07-03, under 510(k) number K791033.

Who is the listed applicant for CAM-10 PVV PORTABLE VOLUME VENTILATOR?

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

What is the FDA product code for CAM-10 PVV PORTABLE VOLUME VENTILATOR?

The FDA product code for CAM-10 PVV PORTABLE VOLUME 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 Lifecare Services, 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 20 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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