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)

MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY

K-Number: K860496 · 1986-03-14

ApplicantXanar, Inc.
Decision Date1986-03-14
Product CodeLNK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY is the device name listed in this FDA 510(k) record. The listed applicant is Xanar, Inc.. It received FDA 510(k) clearance on 1986-03-14 under 510(k) number K860496. The device is classified under product code LNK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY?

MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY is a medical device that received FDA 510(k) clearance on 1986-03-14. The listed applicant is Xanar, Inc.. The 510(k) number is K860496.

When did MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY receive FDA 510(k) clearance?

MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY received FDA 510(k) clearance on 1986-03-14, under 510(k) number K860496.

Who is the listed applicant for MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY?

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

What is the FDA product code for MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY?

The FDA product code for MODEL NY-110 FOR UPPER & LOWER (GU) & PULMONARY is LNK.

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 Xanar, 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.

K861688XANAR CO2 SURGICAL LASER SYSTEM MODEL XAP-15K852436AMBULASEK853620MODEL XA-50 - CO2 SURGICAL LASERK850818CO 2 SURGICAL LASER SYSTEM NA-120K850805CO 2 SURGICAL LASER SYSTEM MODEL NA-40K850804CO 2 SURGICAL LASER SYSTEM NA-30

View all 12 devices →

Related Devices (Code: LNK)

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.

K925395TECHNOMED PULSOLITH 4000 LASER SYSTEMTeknomed, Inc.K901723MDL-2000 LASERTRIPTERCandela Laser Corp.K874255ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI.Minnesota Laser Corp.K874253ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.Minnesota Laser Corp.K880256MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USESharplan Lasers, Inc.K880193MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USESharplan Lasers, 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.

↑