FDA 510(k)

TRACHEOSTOMY CARE KIT

K-Number: K924243 · 1993-06-16

Decision Date1993-06-16

Product CodeJOH

Advisory CommitteeAN

DecisionUnknown

Device Summary

TRACHEOSTOMY CARE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1993-06-16 under 510(k) number K924243. The device is classified under product code JOH. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the TRACHEOSTOMY CARE KIT?

TRACHEOSTOMY CARE KIT is a medical device that received FDA 510(k) clearance on 1993-06-16. The listed applicant is Transidyne General Corp.. The 510(k) number is K924243.

When did TRACHEOSTOMY CARE KIT receive FDA 510(k) clearance?

TRACHEOSTOMY CARE KIT received FDA 510(k) clearance on 1993-06-16, under 510(k) number K924243.

Who is the listed applicant for TRACHEOSTOMY CARE KIT?

The FDA 510(k) record lists Transidyne General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRACHEOSTOMY CARE KIT?

The FDA product code for TRACHEOSTOMY CARE KIT is JOH.

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Other records listing Transidyne General Corp. 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.