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FDA 510(k)

BILE ESCULIN AGAR PLATE

K-Number: K840068 · 1984-01-30

ApplicantOtisville Biotech, Inc.
Decision Date1984-01-30
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BILE ESCULIN AGAR PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Otisville Biotech, Inc.. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K840068. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILE ESCULIN AGAR PLATE?

BILE ESCULIN AGAR PLATE is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K840068.

When did BILE ESCULIN AGAR PLATE receive FDA 510(k) clearance?

BILE ESCULIN AGAR PLATE received FDA 510(k) clearance on 1984-01-30, under 510(k) number K840068.

Who is the listed applicant for BILE ESCULIN AGAR PLATE?

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

What is the FDA product code for BILE ESCULIN AGAR PLATE?

The FDA product code for BILE ESCULIN AGAR PLATE is JSH.

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Other records listing Otisville Biotech, 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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