FDA 510(k)

OCUTOME PARATUBING SET

K-Number: K832938 · 1983-10-19

Decision Date1983-10-19

Product Code

DecisionSubstantially Equivalent

Device Summary

OCUTOME PARATUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Vxtra Corp.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K832938. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OCUTOME PARATUBING SET?

OCUTOME PARATUBING SET is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Vxtra Corp.. The 510(k) number is K832938.

When did OCUTOME PARATUBING SET receive FDA 510(k) clearance?

OCUTOME PARATUBING SET received FDA 510(k) clearance on 1983-10-19, under 510(k) number K832938.

Who is the listed applicant for OCUTOME PARATUBING SET?

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

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Other records listing Vxtra Corp. as applicant

K832980VXTRA OCUTOME KIT K831266MICROSURGICAL KNIFE K830379PHAKO KIT K830385IRRIGATION/ASPIRATION KIT K812620ADJUSTABLE MICROSURGICAL KNIFE K812526MICRO BLADE II

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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.