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FDA 510(k)

DISPOSABLE OCUTOME PROBE

K-Number: K833371 · 1984-01-04

ApplicantCooperVision, Inc.
Decision Date1984-01-04
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE OCUTOME PROBE is the device name listed in this FDA 510(k) record. The listed applicant is CooperVision, Inc.. It received FDA 510(k) clearance on 1984-01-04 under 510(k) number K833371. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE OCUTOME PROBE?

DISPOSABLE OCUTOME PROBE is a medical device that received FDA 510(k) clearance on 1984-01-04. The listed applicant is CooperVision, Inc.. The 510(k) number is K833371.

When did DISPOSABLE OCUTOME PROBE receive FDA 510(k) clearance?

DISPOSABLE OCUTOME PROBE received FDA 510(k) clearance on 1984-01-04, under 510(k) number K833371.

Who is the listed applicant for DISPOSABLE OCUTOME PROBE?

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 DISPOSABLE OCUTOME PROBE?

The FDA product code for DISPOSABLE OCUTOME PROBE is HQE.

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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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