FDA 510(k)

VISI-DRAPE OPHTHALMIC DRAPES

K-Number: K902857 · 1990-07-31

Decision Date1990-07-31

Product CodeHMY

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

VISI-DRAPE OPHTHALMIC DRAPES is the device name listed in this FDA 510(k) record. The listed applicant is Visitec Co.. It received FDA 510(k) clearance on 1990-07-31 under 510(k) number K902857. The device is classified under product code HMY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISI-DRAPE OPHTHALMIC DRAPES?

VISI-DRAPE OPHTHALMIC DRAPES is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Visitec Co.. The 510(k) number is K902857.

When did VISI-DRAPE OPHTHALMIC DRAPES receive FDA 510(k) clearance?

VISI-DRAPE OPHTHALMIC DRAPES received FDA 510(k) clearance on 1990-07-31, under 510(k) number K902857.

Who is the listed applicant for VISI-DRAPE OPHTHALMIC DRAPES?

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

What is the FDA product code for VISI-DRAPE OPHTHALMIC DRAPES?

The FDA product code for VISI-DRAPE OPHTHALMIC DRAPES is HMY.

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Other records listing Visitec Co. as applicant

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Related Devices (Code: HMY)

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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.