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FDA 510(k)

LASER RESISTANT TRACHEAL TUBE (TENTATIVE)

K-Number: K860901 · 1986-06-05

Decision Date1986-06-05
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LASER RESISTANT TRACHEAL TUBE (TENTATIVE) is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Critical Care. It received FDA 510(k) clearance on 1986-06-05 under 510(k) number K860901. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER RESISTANT TRACHEAL TUBE (TENTATIVE)?

LASER RESISTANT TRACHEAL TUBE (TENTATIVE) is a medical device that received FDA 510(k) clearance on 1986-06-05. The listed applicant is Mallinckrodt Critical Care. The 510(k) number is K860901.

When did LASER RESISTANT TRACHEAL TUBE (TENTATIVE) receive FDA 510(k) clearance?

LASER RESISTANT TRACHEAL TUBE (TENTATIVE) received FDA 510(k) clearance on 1986-06-05, under 510(k) number K860901.

Who is the listed applicant for LASER RESISTANT TRACHEAL TUBE (TENTATIVE)?

The FDA 510(k) record lists Mallinckrodt Critical Care as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER RESISTANT TRACHEAL TUBE (TENTATIVE)?

The FDA product code for LASER RESISTANT TRACHEAL TUBE (TENTATIVE) is BTR.

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 Mallinckrodt Critical Care 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.

View all 92 devices →

Related Devices (Code: BTR)

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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