FDA 510(k)

THAYER-MARTIN MEDIUM

K-Number: K791483 · 1979-08-22

ApplicantIsle Media and Sterile Products, Inc.

Decision Date1979-08-22

Product CodeJTY

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

THAYER-MARTIN MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Isle Media and Sterile Products, Inc.. It received FDA 510(k) clearance on 1979-08-22 under 510(k) number K791483. 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 MEDIUM?

THAYER-MARTIN MEDIUM is a medical device that received FDA 510(k) clearance on 1979-08-22. The listed applicant is Isle Media and Sterile Products, Inc.. The 510(k) number is K791483.

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

THAYER-MARTIN MEDIUM received FDA 510(k) clearance on 1979-08-22, under 510(k) number K791483.

Who is the listed applicant for THAYER-MARTIN MEDIUM?

The FDA 510(k) record lists Isle Media and Sterile Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THAYER-MARTIN MEDIUM?

The FDA product code for THAYER-MARTIN MEDIUM is JTY.

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Other records listing Isle Media and Sterile Products, 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.