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FDA 510(k)

INSTRUMENT WIPE AND CORNEAL SHIELD

K-Number: K912576 · 1992-01-31

ApplicantKatena Products, Inc.
Decision Date1992-01-31
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT WIPE AND CORNEAL SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Katena Products, Inc.. It received FDA 510(k) clearance on 1992-01-31 under 510(k) number K912576. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT WIPE AND CORNEAL SHIELD?

INSTRUMENT WIPE AND CORNEAL SHIELD is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Katena Products, Inc.. The 510(k) number is K912576.

When did INSTRUMENT WIPE AND CORNEAL SHIELD receive FDA 510(k) clearance?

INSTRUMENT WIPE AND CORNEAL SHIELD received FDA 510(k) clearance on 1992-01-31, under 510(k) number K912576.

Who is the listed applicant for INSTRUMENT WIPE AND CORNEAL SHIELD?

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

What is the FDA product code for INSTRUMENT WIPE AND CORNEAL SHIELD?

The FDA product code for INSTRUMENT WIPE AND CORNEAL SHIELD is HOY.

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Other records listing Katena Products, Inc. as applicant

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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.

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