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FDA 510(k)

LASER BRONCHOSCOPE SYSTEM

K-Number: K861921 · 1986-06-02

ApplicantPilling Co.
Decision Date1986-06-02
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LASER BRONCHOSCOPE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1986-06-02 under 510(k) number K861921. 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 LASER BRONCHOSCOPE SYSTEM?

LASER BRONCHOSCOPE SYSTEM is a medical device that received FDA 510(k) clearance on 1986-06-02. The listed applicant is Pilling Co.. The 510(k) number is K861921.

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

LASER BRONCHOSCOPE SYSTEM received FDA 510(k) clearance on 1986-06-02, under 510(k) number K861921.

Who is the listed applicant for LASER BRONCHOSCOPE SYSTEM?

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

What is the FDA product code for LASER BRONCHOSCOPE SYSTEM?

The FDA product code for LASER BRONCHOSCOPE SYSTEM is LLO.

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Other records listing Pilling Co. 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.

K934427PILLING LAPAROSCOPIC INSTRUMENTATIONK925370TRIANGULAR JAW MICROLARYNGEAL FORCEPSK925198KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTRK922971NO-SCALPEL VASCETOMY INSTRUMENTSK914015CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMPK911099MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE

View all 39 devices →

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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