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FDA 510(k)

YEP (YEAST EXTRACT PHOSPHATE) AGAR

K-Number: K863526 · 1986-09-19

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic
Decision Date1986-09-19
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

YEP (YEAST EXTRACT PHOSPHATE) AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1986-09-19 under 510(k) number K863526. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YEP (YEAST EXTRACT PHOSPHATE) AGAR?

YEP (YEAST EXTRACT PHOSPHATE) AGAR is a medical device that received FDA 510(k) clearance on 1986-09-19. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K863526.

When did YEP (YEAST EXTRACT PHOSPHATE) AGAR receive FDA 510(k) clearance?

YEP (YEAST EXTRACT PHOSPHATE) AGAR received FDA 510(k) clearance on 1986-09-19, under 510(k) number K863526.

Who is the listed applicant for YEP (YEAST EXTRACT PHOSPHATE) AGAR?

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

What is the FDA product code for YEP (YEAST EXTRACT PHOSPHATE) AGAR?

The FDA product code for YEP (YEAST EXTRACT PHOSPHATE) AGAR is JSJ.

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Related Devices (Code: JSJ)

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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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