FDA 510(k)

H55 HYDROPHILIC CONTACT LENS

K-Number: K942214 · 1994-07-28

Decision Date1994-07-28

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

H55 HYDROPHILIC CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Martin S. Knopf Assoc., Inc.. It received FDA 510(k) clearance on 1994-07-28 under 510(k) number K942214. 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 H55 HYDROPHILIC CONTACT LENS?

H55 HYDROPHILIC CONTACT LENS is a medical device that received FDA 510(k) clearance on 1994-07-28. The listed applicant is Martin S. Knopf Assoc., Inc.. The 510(k) number is K942214.

When did H55 HYDROPHILIC CONTACT LENS receive FDA 510(k) clearance?

H55 HYDROPHILIC CONTACT LENS received FDA 510(k) clearance on 1994-07-28, under 510(k) number K942214.

Who is the listed applicant for H55 HYDROPHILIC CONTACT LENS?

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

What is the FDA product code for H55 HYDROPHILIC CONTACT LENS?

The FDA product code for H55 HYDROPHILIC CONTACT LENS 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.