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FDA 510(k)

TRACHEOSTOMY KIT

K-Number: K925288 · 1993-08-27

ApplicantAjs Medical Co., Inc.
Decision Date1993-08-27
Product CodeJOH
Advisory CommitteeAN
DecisionUnknown

Device Summary

TRACHEOSTOMY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ajs Medical Co., Inc.. It received FDA 510(k) clearance on 1993-08-27 under 510(k) number K925288. 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 KIT?

TRACHEOSTOMY KIT is a medical device that received FDA 510(k) clearance on 1993-08-27. The listed applicant is Ajs Medical Co., Inc.. The 510(k) number is K925288.

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

TRACHEOSTOMY KIT received FDA 510(k) clearance on 1993-08-27, under 510(k) number K925288.

Who is the listed applicant for TRACHEOSTOMY KIT?

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

What is the FDA product code for TRACHEOSTOMY KIT?

The FDA product code for TRACHEOSTOMY KIT is JOH.

Related Clinical Trials

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Other records listing Ajs Medical Co., 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.

K914471NEEDLECRIC

Related Devices (Code: JOH)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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