Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-

K-Number: K850432 · 1985-02-15

ApplicantCooper Lasersonics, Inc.
Decision Date1985-02-15
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- is the device name listed in this FDA 510(k) record. The listed applicant is Cooper Lasersonics, Inc.. It received FDA 510(k) clearance on 1985-02-15 under 510(k) number K850432. 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 BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-?

LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- is a medical device that received FDA 510(k) clearance on 1985-02-15. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K850432.

When did LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- receive FDA 510(k) clearance?

LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- received FDA 510(k) clearance on 1985-02-15, under 510(k) number K850432.

Who is the listed applicant for LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-?

The FDA 510(k) record lists Cooper Lasersonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS-?

The FDA product code for LASER BENIGN & MALIGNANT PULMONARY OBSTRUCTIONS- is LLO.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Cooper Lasersonics, Inc. 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.

K880808ILLUMINA MODEL 40 CO2 LASER FOR GENERAL/PLASTIC SUK880807ILLUMINA MODEL 25 CO2 LASER FOR GENERAL/PLASTIC SUK880427ILLUMINA 40 CO2 LASER SYSTEMK880428ILLUMINA 25 CO2 LASER SYSTEMK880429ILLUMINA 55 CO2 LASER SYSTEMK880809ILLUMINA MODEL 55 CO2 LASER FOR GENERAL/PLASTIC SU

View all 54 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.

↑