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FDA 510(k)

ND:YAG LASER PULMONARY OBSTRUCTION

K-Number: K844458 · 1985-01-03

ApplicantEndo Lase, Inc.
Decision Date1985-01-03
Product Code
DecisionSubstantially Equivalent

Device Summary

ND:YAG LASER PULMONARY OBSTRUCTION is the device name listed in this FDA 510(k) record. The listed applicant is Endo Lase, Inc.. It received FDA 510(k) clearance on 1985-01-03 under 510(k) number K844458. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND:YAG LASER PULMONARY OBSTRUCTION?

ND:YAG LASER PULMONARY OBSTRUCTION is a medical device that received FDA 510(k) clearance on 1985-01-03. The listed applicant is Endo Lase, Inc.. The 510(k) number is K844458.

When did ND:YAG LASER PULMONARY OBSTRUCTION receive FDA 510(k) clearance?

ND:YAG LASER PULMONARY OBSTRUCTION received FDA 510(k) clearance on 1985-01-03, under 510(k) number K844458.

Who is the listed applicant for ND:YAG LASER PULMONARY OBSTRUCTION?

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

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.

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Other records listing Endo Lase, 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.

K853900ENDO-LASE CD40 FOR NEUROSURGERYK853878ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERYK855093MEDILAS 2 ND:YAG LASER SURGERY SYSTEMK853903ENDO-LASE CD40 CO2 FOR GYNECOLOGYK853876ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGYK853901ENDO-LASE CD 40 FOR DERMATOLOGY

View all 24 devices →

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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