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FDA 510(k)

CO2 LASER BRONCHOSCOPE SYSTEM

K-Number: K861583 · 1986-05-21

ApplicantRichard Wolf Medical Instruments Corp.
Decision Date1986-05-21
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CO2 LASER BRONCHOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1986-05-21 under 510(k) number K861583. The device is classified under product code LLO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CO2 LASER BRONCHOSCOPE SYSTEM?

CO2 LASER BRONCHOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1986-05-21. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K861583.

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

CO2 LASER BRONCHOSCOPE SYSTEM received FDA 510(k) clearance on 1986-05-21, under 510(k) number K861583.

Who is the listed applicant for CO2 LASER BRONCHOSCOPE SYSTEM?

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

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

The FDA product code for CO2 LASER BRONCHOSCOPE SYSTEM is LLO.

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Other records listing Richard Wolf Medical Instruments Corp. as applicant

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K151282core nova Complete Operating Room EndoscopyK130423THE RICHARD WOLF ENDOCAM LOGIC HD CAMERA SYSTEM 5525K121724ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2K120898KEYPORT SYSTEM, INCLUDES: KEYPORT SILICONE SEALING INSERT 8850XXX KEYPORT TRUCAR 8850XX KEYPORT TROCAR 8850XX SEALING CAK090776MEGAPULSE LASER SYSTEM AND FIBERSK080617POWER DRIVE ART1 2304 WITH MOTOR HANDLES, TOOLS AND ACCESSORIES

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Related Devices (Code: LLO)

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.

K884815SLT CLMD CONTACT LASERSurgical Laser Technologies, Inc.K881499SURGILASE YAG 100 FOR GYNECOLOGY USESurgilase, Inc.K880592LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USELaser Peripherals, LLCK880170MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONSCooper Lasersonics, Inc.K874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSMinnesota Laser Corp.K875104SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USELaserguide

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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