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FDA 510(k)

NOVALENS/NOVAWET PERCEPTION AND VANGUARD

K-Number: K942533 · 1994-08-05

ApplicantOcutec Corporation, Inc.
Decision Date1994-08-05
Product CodeHQD
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NOVALENS/NOVAWET PERCEPTION AND VANGUARD is the device name listed in this FDA 510(k) record. The listed applicant is Ocutec Corporation, Inc.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K942533. The device is classified under product code HQD. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVALENS/NOVAWET PERCEPTION AND VANGUARD?

NOVALENS/NOVAWET PERCEPTION AND VANGUARD is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Ocutec Corporation, Inc.. The 510(k) number is K942533.

When did NOVALENS/NOVAWET PERCEPTION AND VANGUARD receive FDA 510(k) clearance?

NOVALENS/NOVAWET PERCEPTION AND VANGUARD received FDA 510(k) clearance on 1994-08-05, under 510(k) number K942533.

Who is the listed applicant for NOVALENS/NOVAWET PERCEPTION AND VANGUARD?

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

What is the FDA product code for NOVALENS/NOVAWET PERCEPTION AND VANGUARD?

The FDA product code for NOVALENS/NOVAWET PERCEPTION AND VANGUARD is HQD.

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Related Devices (Code: HQD)

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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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