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FDA 510(k)

THAYER-MARTIN, MODIFIED

K-Number: K830061 · 1983-02-09

ApplicantbioMerieux, Inc.
Decision Date1983-02-09
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER-MARTIN, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 1983-02-09 under 510(k) number K830061. 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, MODIFIED?

THAYER-MARTIN, MODIFIED is a medical device that received FDA 510(k) clearance on 1983-02-09. The listed applicant is bioMerieux, Inc.. The 510(k) number is K830061.

When did THAYER-MARTIN, MODIFIED receive FDA 510(k) clearance?

THAYER-MARTIN, MODIFIED received FDA 510(k) clearance on 1983-02-09, under 510(k) number K830061.

Who is the listed applicant for THAYER-MARTIN, MODIFIED?

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

What is the FDA product code for THAYER-MARTIN, MODIFIED?

The FDA product code for THAYER-MARTIN, MODIFIED is 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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