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FDA 510(k)

CO2 LASER BRONCHOSCOPE SET

K-Number: K870063 · 1987-03-09

ApplicantTti Medical
Decision Date1987-03-09
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CO2 LASER BRONCHOSCOPE SET is the device name listed in this FDA 510(k) record. The listed applicant is Tti Medical. It received FDA 510(k) clearance on 1987-03-09 under 510(k) number K870063. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 LASER BRONCHOSCOPE SET?

CO2 LASER BRONCHOSCOPE SET is a medical device that received FDA 510(k) clearance on 1987-03-09. The listed applicant is Tti Medical. The 510(k) number is K870063.

When did CO2 LASER BRONCHOSCOPE SET receive FDA 510(k) clearance?

CO2 LASER BRONCHOSCOPE SET received FDA 510(k) clearance on 1987-03-09, under 510(k) number K870063.

Who is the listed applicant for CO2 LASER BRONCHOSCOPE SET?

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

What is the FDA product code for CO2 LASER BRONCHOSCOPE SET?

The FDA product code for CO2 LASER BRONCHOSCOPE SET is EOQ.

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 Tti Medical 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 9 devices →

Related Devices (Code: EOQ)

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

View on FDA Database →

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

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