FDA 510(k)

METRO 55G TORIC & SPHERICAL

K-Number: K953199 · 1995-12-11

Decision Date1995-12-11

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

METRO 55G TORIC & SPHERICAL is the device name listed in this FDA 510(k) record. The listed applicant is Metrosoft, Inc.. It received FDA 510(k) clearance on 1995-12-11 under 510(k) number K953199. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the METRO 55G TORIC & SPHERICAL?

METRO 55G TORIC & SPHERICAL is a medical device that received FDA 510(k) clearance on 1995-12-11. The listed applicant is Metrosoft, Inc.. The 510(k) number is K953199.

When did METRO 55G TORIC & SPHERICAL receive FDA 510(k) clearance?

METRO 55G TORIC & SPHERICAL received FDA 510(k) clearance on 1995-12-11, under 510(k) number K953199.

Who is the listed applicant for METRO 55G TORIC & SPHERICAL?

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

What is the FDA product code for METRO 55G TORIC & SPHERICAL?

The FDA product code for METRO 55G TORIC & SPHERICAL is LPL.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Metrosoft, Inc. as applicant

K983021METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC

Related Devices (Code: LPL)

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.