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FDA 510(k)

OVES CERVICAL CAP

K-Number: K993953 · 2000-03-21

ApplicantVeos , Ltd.
Decision Date2000-03-21
Product CodeHDR
Advisory CommitteeOB
DecisionUnknown

Device Summary

OVES CERVICAL CAP is the device name listed in this FDA 510(k) record. The listed applicant is Veos , Ltd.. It received FDA 510(k) clearance on 2000-03-21 under 510(k) number K993953. The device is classified under product code HDR. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the OVES CERVICAL CAP?

OVES CERVICAL CAP is a medical device that received FDA 510(k) clearance on 2000-03-21. The listed applicant is Veos , Ltd.. The 510(k) number is K993953.

When did OVES CERVICAL CAP receive FDA 510(k) clearance?

OVES CERVICAL CAP received FDA 510(k) clearance on 2000-03-21, under 510(k) number K993953.

Who is the listed applicant for OVES CERVICAL CAP?

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

What is the FDA product code for OVES CERVICAL CAP?

The FDA product code for OVES CERVICAL CAP is HDR.

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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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