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FDA 510(k)

AUTOMATIC TANGENT SCREEN 50

K-Number: K832800 · 1983-09-29

ApplicantCooperVision, Inc.
Decision Date1983-09-29
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AUTOMATIC TANGENT SCREEN 50 is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832800. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUTOMATIC TANGENT SCREEN 50?

AUTOMATIC TANGENT SCREEN 50 is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is CooperVision, Inc.. The 510(k) number is K832800.

When did AUTOMATIC TANGENT SCREEN 50 receive FDA 510(k) clearance?

AUTOMATIC TANGENT SCREEN 50 received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832800.

Who is the listed applicant for AUTOMATIC TANGENT SCREEN 50?

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 AUTOMATIC TANGENT SCREEN 50?

The FDA product code for AUTOMATIC TANGENT SCREEN 50 is HOO.

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Related Devices (Code: HOO)

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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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