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FDA 510(k)

VISION TWO, ONE/10 ONE/20 &24

K-Number: K832895 · 1983-12-08

ApplicantComtal Corp.
Decision Date1983-12-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISION TWO, ONE/10 ONE/20 &24 is the device name listed in this FDA 510(k) record. The listed applicant is Comtal Corp.. It received FDA 510(k) clearance on 1983-12-08 under 510(k) number K832895. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISION TWO, ONE/10 ONE/20 &24?

VISION TWO, ONE/10 ONE/20 &24 is a medical device that received FDA 510(k) clearance on 1983-12-08. The listed applicant is Comtal Corp.. The 510(k) number is K832895.

When did VISION TWO, ONE/10 ONE/20 &24 receive FDA 510(k) clearance?

VISION TWO, ONE/10 ONE/20 &24 received FDA 510(k) clearance on 1983-12-08, under 510(k) number K832895.

Who is the listed applicant for VISION TWO, ONE/10 ONE/20 &24?

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

What is the FDA product code for VISION TWO, ONE/10 ONE/20 &24?

The FDA product code for VISION TWO, ONE/10 ONE/20 &24 is LLZ.

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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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