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FDA 510(k)

TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER

K-Number: K962078 · 1996-10-11

Decision Date1996-10-11
Product CodeJOH
Advisory CommitteeAN
DecisionUnknown

Device Summary

TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Continental Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1996-10-11 under 510(k) number K962078. 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 CLEANING TRAY W/SUCTION CATHETER?

TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER is a medical device that received FDA 510(k) clearance on 1996-10-11. The listed applicant is Continental Medical Laboratories, Inc.. The 510(k) number is K962078.

When did TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER receive FDA 510(k) clearance?

TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER received FDA 510(k) clearance on 1996-10-11, under 510(k) number K962078.

Who is the listed applicant for TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER?

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

What is the FDA product code for TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER?

The FDA product code for TRACHEOSTOMY CLEANING TRAY W/SUCTION CATHETER is JOH.

Related Clinical Trials

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.

Other records listing Continental Medical Laboratories, 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.

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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.

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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