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FDA 510(k)

ENTEROCOCCUS SCREENING MEDIUM

K-Number: K951539 · 1995-06-13

ApplicantBecton Dickinson Microbiology Systems
Decision Date1995-06-13
Product CodeJWY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ENTEROCOCCUS SCREENING MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Microbiology Systems. It received FDA 510(k) clearance on 1995-06-13 under 510(k) number K951539. The device is classified under product code JWY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENTEROCOCCUS SCREENING MEDIUM?

ENTEROCOCCUS SCREENING MEDIUM is a medical device that received FDA 510(k) clearance on 1995-06-13. The listed applicant is Becton Dickinson Microbiology Systems. The 510(k) number is K951539.

When did ENTEROCOCCUS SCREENING MEDIUM receive FDA 510(k) clearance?

ENTEROCOCCUS SCREENING MEDIUM received FDA 510(k) clearance on 1995-06-13, under 510(k) number K951539.

Who is the listed applicant for ENTEROCOCCUS SCREENING MEDIUM?

The FDA 510(k) record lists Becton Dickinson Microbiology Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENTEROCOCCUS SCREENING MEDIUM?

The FDA product code for ENTEROCOCCUS SCREENING MEDIUM is JWY.

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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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