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FDA 510(k)

DICON GLAUCOMA DIAG. CENTER 2000 SERIES

K-Number: K832142 · 1983-08-01

ApplicantCooperVision, Inc.
Decision Date1983-08-01
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DICON GLAUCOMA DIAG. CENTER 2000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1983-08-01 under 510(k) number K832142. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DICON GLAUCOMA DIAG. CENTER 2000 SERIES?

DICON GLAUCOMA DIAG. CENTER 2000 SERIES is a medical device that received FDA 510(k) clearance on 1983-08-01. The listed applicant is CooperVision, Inc.. The 510(k) number is K832142.

When did DICON GLAUCOMA DIAG. CENTER 2000 SERIES receive FDA 510(k) clearance?

DICON GLAUCOMA DIAG. CENTER 2000 SERIES received FDA 510(k) clearance on 1983-08-01, under 510(k) number K832142.

Who is the listed applicant for DICON GLAUCOMA DIAG. CENTER 2000 SERIES?

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

What is the FDA product code for DICON GLAUCOMA DIAG. CENTER 2000 SERIES?

The FDA product code for DICON GLAUCOMA DIAG. CENTER 2000 SERIES is HPT.

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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.

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