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FDA 510(k)

VDC

K-Number: K791756 · 1979-11-27

ApplicantLife Sciences Manufacturing, Inc.
Decision Date1979-11-27
Product CodeDXG
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VDC is the device name listed in this FDA 510(k) record. The listed applicant is Life Sciences Manufacturing, Inc.. It received FDA 510(k) clearance on 1979-11-27 under 510(k) number K791756. The device is classified under product code DXG. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VDC?

VDC is a medical device that received FDA 510(k) clearance on 1979-11-27. The listed applicant is Life Sciences Manufacturing, Inc.. The 510(k) number is K791756.

When did VDC receive FDA 510(k) clearance?

VDC received FDA 510(k) clearance on 1979-11-27, under 510(k) number K791756.

Who is the listed applicant for VDC?

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

What is the FDA product code for VDC?

The FDA product code for VDC is DXG.

Other records listing Life Sciences Manufacturing, 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.

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Related Devices (Code: DXG)

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.

K253092Argos Infinity (Rev. 1.0)Retia Medical Systems, Inc.K251275VitalStream ART Connect; VitalStream-HemoCaretaker MedicalK232048Cogent™ Hemodynamic Monitoring System; Cogent™ HMSIcu MedicalK212529Hypotension Decision Assist Model HDA-OR2Directed Systems, Ltd.K192169PulsioFlex Monitoring System with ProAQT SensorPulsion Medical Systems SEK193179EV1000 Clinical PlatformEdwards Lifesciences, LLC

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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