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FDA 510(k)

VENTREX DATA REDUCTION & QUAL. CONTR. SY

K-Number: K812357 · 1981-09-01

ApplicantVentrex Laboratories, Inc.
Decision Date1981-09-01
Product CodeJPK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

VENTREX DATA REDUCTION & QUAL. CONTR. SY 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 1981-09-01 under 510(k) number K812357. The device is classified under product code JPK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTREX DATA REDUCTION & QUAL. CONTR. SY?

VENTREX DATA REDUCTION & QUAL. CONTR. SY is a medical device that received FDA 510(k) clearance on 1981-09-01. The listed applicant is Ventrex Laboratories, Inc.. The 510(k) number is K812357.

When did VENTREX DATA REDUCTION & QUAL. CONTR. SY receive FDA 510(k) clearance?

VENTREX DATA REDUCTION & QUAL. CONTR. SY received FDA 510(k) clearance on 1981-09-01, under 510(k) number K812357.

Who is the listed applicant for VENTREX DATA REDUCTION & QUAL. CONTR. SY?

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 VENTREX DATA REDUCTION & QUAL. CONTR. SY?

The FDA product code for VENTREX DATA REDUCTION & QUAL. CONTR. SY is JPK.

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Other records listing Ventrex Laboratories, Inc. as applicant

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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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