FDA 510(k)

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

K-Number: K983021 · 1998-11-13

Decision Date1998-11-13

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC is the device name listed in this FDA 510(k) record. The listed applicant is Metrosoft, Inc.. It received FDA 510(k) clearance on 1998-11-13 under 510(k) number K983021. 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 METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC?

METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC is a medical device that received FDA 510(k) clearance on 1998-11-13. The listed applicant is Metrosoft, Inc.. The 510(k) number is K983021.

When did METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC receive FDA 510(k) clearance?

METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC received FDA 510(k) clearance on 1998-11-13, under 510(k) number K983021.

Who is the listed applicant for METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC?

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

The FDA product code for METROSOFT II, METROSOFT TORIC, METROLITE, METROTINT, SATUREYES, SATUREYES TORIC, SATUREYES LITE, SATUREYES LITE TORIC is LPL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.