FDA 510(k)

ETO METHOD - STERILIZE INTRAOCULAR LENS

K-Number: K761178 · 1976-12-15

Decision Date1976-12-15

Product Code

DecisionSubstantially Equivalent

Device Summary

ETO METHOD - STERILIZE INTRAOCULAR LENS is the device name listed in this FDA 510(k) record. The listed applicant is Medical Workshop. It received FDA 510(k) clearance on 1976-12-15 under 510(k) number K761178. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETO METHOD - STERILIZE INTRAOCULAR LENS?

ETO METHOD - STERILIZE INTRAOCULAR LENS is a medical device that received FDA 510(k) clearance on 1976-12-15. The listed applicant is Medical Workshop. The 510(k) number is K761178.

When did ETO METHOD - STERILIZE INTRAOCULAR LENS receive FDA 510(k) clearance?

ETO METHOD - STERILIZE INTRAOCULAR LENS received FDA 510(k) clearance on 1976-12-15, under 510(k) number K761178.

Who is the listed applicant for ETO METHOD - STERILIZE INTRAOCULAR LENS?

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

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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.