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FDA 510(k)

CORD, ENTEROBACTERIACEAE BIOCHEMICAL

K-Number: K782056 · 1979-01-26

ApplicantVitek Systems, Inc.
Decision Date1979-01-26
Product CodeJSS
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CORD, ENTEROBACTERIACEAE BIOCHEMICAL is the device name listed in this FDA 510(k) record. The listed applicant is Vitek Systems, Inc.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K782056. The device is classified under product code JSS. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORD, ENTEROBACTERIACEAE BIOCHEMICAL?

CORD, ENTEROBACTERIACEAE BIOCHEMICAL is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Vitek Systems, Inc.. The 510(k) number is K782056.

When did CORD, ENTEROBACTERIACEAE BIOCHEMICAL receive FDA 510(k) clearance?

CORD, ENTEROBACTERIACEAE BIOCHEMICAL received FDA 510(k) clearance on 1979-01-26, under 510(k) number K782056.

Who is the listed applicant for CORD, ENTEROBACTERIACEAE BIOCHEMICAL?

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

What is the FDA product code for CORD, ENTEROBACTERIACEAE BIOCHEMICAL?

The FDA product code for CORD, ENTEROBACTERIACEAE BIOCHEMICAL is JSS.

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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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