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FDA 510(k)

DYNA INTRA-LIMBAL LENS

K-Number: K020006 · 2002-03-29

Decision Date2002-03-29
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DYNA INTRA-LIMBAL LENS is the device name listed in this FDA 510(k) record. The listed applicant is Lens Dynamics, Inc.. It received FDA 510(k) clearance on 2002-03-29 under 510(k) number K020006. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DYNA INTRA-LIMBAL LENS?

DYNA INTRA-LIMBAL LENS is a medical device that received FDA 510(k) clearance on 2002-03-29. The listed applicant is Lens Dynamics, Inc.. The 510(k) number is K020006.

When did DYNA INTRA-LIMBAL LENS receive FDA 510(k) clearance?

DYNA INTRA-LIMBAL LENS received FDA 510(k) clearance on 2002-03-29, under 510(k) number K020006.

Who is the listed applicant for DYNA INTRA-LIMBAL LENS?

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

What is the FDA product code for DYNA INTRA-LIMBAL LENS?

The FDA product code for DYNA INTRA-LIMBAL LENS is HQD.

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.

Related Devices (Code: HQD)

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.

Official Source

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