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FDA 510(k)

ATL 225 MW TRAIL LENS SET

K-Number: K852548 · 1985-07-31

ApplicantAscon Medical Instruments, Ltd.
Decision Date1985-07-31
Product CodeHPA
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ATL 225 MW TRAIL LENS SET is the device name listed in this FDA 510(k) record. The listed applicant is Ascon Medical Instruments, Ltd.. It received FDA 510(k) clearance on 1985-07-31 under 510(k) number K852548. The device is classified under product code HPA. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATL 225 MW TRAIL LENS SET?

ATL 225 MW TRAIL LENS SET is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is Ascon Medical Instruments, Ltd.. The 510(k) number is K852548.

When did ATL 225 MW TRAIL LENS SET receive FDA 510(k) clearance?

ATL 225 MW TRAIL LENS SET received FDA 510(k) clearance on 1985-07-31, under 510(k) number K852548.

Who is the listed applicant for ATL 225 MW TRAIL LENS SET?

The FDA 510(k) record lists Ascon Medical Instruments, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATL 225 MW TRAIL LENS SET?

The FDA product code for ATL 225 MW TRAIL LENS SET is HPA.

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 Ascon Medical Instruments, Ltd. 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.

K852054CONTACT LENS LOUPE, INSPETION LOUPEK852055ASCON OPHTHALMIC SPONGEK852057ASCON SURGICAL INSTRUMENTSK852126ATF 101 TRAIL FRAMEK852056ACC CROSS CYLINDERS

Related Devices (Code: HPA)

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.

K852126ATF 101 TRAIL FRAMEAscon Medical Instruments, Ltd.K841768WOODLYN LIGHTWEIGHT TRIAL FRAMEWoodlyn, Inc.K833669IMAGE DEFLECTORMichael OnufrykK821084UNIVERSAL TRIAL FRAMEEMedical Equipment Designs, 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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