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FDA 510(k)

TRACHEAL TUBE LASER SHIELD KIT

K-Number: K874679 · 1988-04-11

Decision Date1988-04-11
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRACHEAL TUBE LASER SHIELD KIT is the device name listed in this FDA 510(k) record. The listed applicant is Americal Corp.. It received FDA 510(k) clearance on 1988-04-11 under 510(k) number K874679. 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 TRACHEAL TUBE LASER SHIELD KIT?

TRACHEAL TUBE LASER SHIELD KIT is a medical device that received FDA 510(k) clearance on 1988-04-11. The listed applicant is Americal Corp.. The 510(k) number is K874679.

When did TRACHEAL TUBE LASER SHIELD KIT receive FDA 510(k) clearance?

TRACHEAL TUBE LASER SHIELD KIT received FDA 510(k) clearance on 1988-04-11, under 510(k) number K874679.

Who is the listed applicant for TRACHEAL TUBE LASER SHIELD KIT?

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

What is the FDA product code for TRACHEAL TUBE LASER SHIELD KIT?

The FDA product code for TRACHEAL TUBE LASER SHIELD KIT 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 Americal Corp. 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.

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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