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FDA 510(k)

MPORT FOLDABLE LENS PLACEMENT SYSTEM

K-Number: K970727 · 1997-12-17

ApplicantChiron Vision Corp.
Decision Date1997-12-17
Product CodeMSS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MPORT FOLDABLE LENS PLACEMENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Vision Corp.. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K970727. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MPORT FOLDABLE LENS PLACEMENT SYSTEM?

MPORT FOLDABLE LENS PLACEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Chiron Vision Corp.. The 510(k) number is K970727.

When did MPORT FOLDABLE LENS PLACEMENT SYSTEM receive FDA 510(k) clearance?

MPORT FOLDABLE LENS PLACEMENT SYSTEM received FDA 510(k) clearance on 1997-12-17, under 510(k) number K970727.

Who is the listed applicant for MPORT FOLDABLE LENS PLACEMENT SYSTEM?

The FDA 510(k) record lists Chiron Vision Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MPORT FOLDABLE LENS PLACEMENT SYSTEM?

The FDA product code for MPORT FOLDABLE LENS PLACEMENT SYSTEM is MSS.

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Other records listing Chiron Vision Corp. as applicant

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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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