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FDA 510(k)

MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS

K-Number: K880170 · 1988-03-24

ApplicantCooper Lasersonics, Inc.
Decision Date1988-03-24
Product CodeLLO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 4900 ND:YAG LASER FOR 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 1988-03-24 under 510(k) number K880170. 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 MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS?

MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS is a medical device that received FDA 510(k) clearance on 1988-03-24. The listed applicant is Cooper Lasersonics, Inc.. The 510(k) number is K880170.

When did MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS receive FDA 510(k) clearance?

MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS received FDA 510(k) clearance on 1988-03-24, under 510(k) number K880170.

Who is the listed applicant for MODEL 4900 ND:YAG LASER FOR 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 MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS?

The FDA product code for MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS is LLO.

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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

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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, LLCK874254ND:YAG SURGICAL LASER FOR PULMONARY APPLICATIONSMinnesota Laser Corp.K875104SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USELaserguideK871876MODEL 5050 SURGILASER FOR PULMONARY USELasermatic, Inc.

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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