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FDA 510(k)

VAST VENTREX RAST ALL

K-Number: K841651 · 1984-06-01

ApplicantVentrex Laboratories, Inc.
Decision Date1984-06-01
Product CodeDGC
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

VAST VENTREX RAST ALL is the device name listed in this FDA 510(k) record. The listed applicant is Ventrex Laboratories, Inc.. It received FDA 510(k) clearance on 1984-06-01 under 510(k) number K841651. The device is classified under product code DGC. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAST VENTREX RAST ALL?

VAST VENTREX RAST ALL is a medical device that received FDA 510(k) clearance on 1984-06-01. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K841651.

When did VAST VENTREX RAST ALL receive FDA 510(k) clearance?

VAST VENTREX RAST ALL received FDA 510(k) clearance on 1984-06-01, under 510(k) number K841651.

Who is the listed applicant for VAST VENTREX RAST ALL?

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

What is the FDA product code for VAST VENTREX RAST ALL?

The FDA product code for VAST VENTREX RAST ALL is DGC.

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Other records listing Ventrex Laboratories, Inc. as applicant

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Related Devices (Code: DGC)

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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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