Decision Date2002-04-03
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
RIGID GAS PERMEABLE CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Incorporated. It received FDA 510(k) clearance on 2002-04-03 under 510(k) number K013762. 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 RIGID GAS PERMEABLE CONTACT LENS?
RIGID GAS PERMEABLE CONTACT LENS is a medical device that received FDA 510(k) clearance on 2002-04-03. The listed applicant is Bausch & Lomb, Incorporated. The 510(k) number is K013762.
When did RIGID GAS PERMEABLE CONTACT LENS receive FDA 510(k) clearance?
RIGID GAS PERMEABLE CONTACT LENS received FDA 510(k) clearance on 2002-04-03, under 510(k) number K013762.
Who is the listed applicant for RIGID GAS PERMEABLE CONTACT LENS?
The FDA 510(k) record lists Bausch & Lomb, Incorporated as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RIGID GAS PERMEABLE CONTACT LENS?
The FDA product code for RIGID GAS PERMEABLE CONTACT LENS is HQD.
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Official Source
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