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FDA 510(k)

LASER BRONCHOSCOPE

K-Number: K822136 · 1982-08-16

Decision Date1982-08-16
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LASER BRONCHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Laser Industries of Tel Aviv. It received FDA 510(k) clearance on 1982-08-16 under 510(k) number K822136. 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 LASER BRONCHOSCOPE?

LASER BRONCHOSCOPE is a medical device that received FDA 510(k) clearance on 1982-08-16. The listed applicant is Laser Industries of Tel Aviv. The 510(k) number is K822136.

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

LASER BRONCHOSCOPE received FDA 510(k) clearance on 1982-08-16, under 510(k) number K822136.

Who is the listed applicant for LASER BRONCHOSCOPE?

The FDA 510(k) record lists Laser Industries of Tel Aviv as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER BRONCHOSCOPE?

The FDA product code for LASER BRONCHOSCOPE 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.

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

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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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