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FDA 510(k)

THAYER-MARTIN AGAR PLATE

K-Number: K840067 · 1984-02-13

ApplicantOtisville Biotech, Inc.
Decision Date1984-02-13
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER-MARTIN 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 1984-02-13 under 510(k) number K840067. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THAYER-MARTIN AGAR PLATE?

THAYER-MARTIN AGAR PLATE is a medical device that received FDA 510(k) clearance on 1984-02-13. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K840067.

When did THAYER-MARTIN AGAR PLATE receive FDA 510(k) clearance?

THAYER-MARTIN AGAR PLATE received FDA 510(k) clearance on 1984-02-13, under 510(k) number K840067.

Who is the listed applicant for THAYER-MARTIN 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 THAYER-MARTIN AGAR PLATE?

The FDA product code for THAYER-MARTIN AGAR PLATE is JTY.

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Other records listing Otisville Biotech, Inc. as applicant

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Related Devices (Code: JTY)

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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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