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FDA 510(k)

BIOTIS MARTIN LEWIS AGAR

K-Number: K843817 · 1984-10-10

ApplicantOtisville Biotech, Inc.
Decision Date1984-10-10
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

BIOTIS MARTIN LEWIS AGAR 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 1984-10-10 under 510(k) number K843817. 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 BIOTIS MARTIN LEWIS AGAR?

BIOTIS MARTIN LEWIS AGAR is a medical device that received FDA 510(k) clearance on 1984-10-10. The listed applicant is Otisville Biotech, Inc.. The 510(k) number is K843817.

When did BIOTIS MARTIN LEWIS AGAR receive FDA 510(k) clearance?

BIOTIS MARTIN LEWIS AGAR received FDA 510(k) clearance on 1984-10-10, under 510(k) number K843817.

Who is the listed applicant for BIOTIS MARTIN LEWIS AGAR?

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 BIOTIS MARTIN LEWIS AGAR?

The FDA product code for BIOTIS MARTIN LEWIS AGAR is JTY.

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Other records listing Otisville Biotech, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K862397BIOTIS DECARBOXYLASE MEDIA, LYSINEK862393BIOTIS LITMUS MILKK862398BIOTIS DECARBOXYLASE MEDIA, ORNITHINEK862390BIOTIS BORDET GENGOU AGARK862388BIOTIS TCBS AGARK862392BIOTIS MOTILITY TEST MEDIUM

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Related Devices (Code: JTY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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