FDA 510(k)

KNIFE, TROUTMAN CORNEAL SMALL

K-Number: K760187 · 1976-08-04

ApplicantV. Mueller O.V. Baxter Healthcare Corp.

Decision Date1976-08-04

Product CodeHNN

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

KNIFE, TROUTMAN CORNEAL SMALL is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760187. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNIFE, TROUTMAN CORNEAL SMALL?

KNIFE, TROUTMAN CORNEAL SMALL is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760187.

When did KNIFE, TROUTMAN CORNEAL SMALL receive FDA 510(k) clearance?

KNIFE, TROUTMAN CORNEAL SMALL received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760187.

Who is the listed applicant for KNIFE, TROUTMAN CORNEAL SMALL?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KNIFE, TROUTMAN CORNEAL SMALL?

The FDA product code for KNIFE, TROUTMAN CORNEAL SMALL is HNN.

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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.