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FDA 510(k)

EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY

K-Number: K001576 · 2000-12-28

ApplicantProsurg, Inc.
Decision Date2000-12-28
Product CodeNBV
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY is the device name listed in this FDA 510(k) record. The listed applicant is Prosurg, Inc.. It received FDA 510(k) clearance on 2000-12-28 under 510(k) number K001576. The device is classified under product code NBV. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY?

EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY is a medical device that received FDA 510(k) clearance on 2000-12-28. The listed applicant is Prosurg, Inc.. The 510(k) number is K001576.

When did EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY receive FDA 510(k) clearance?

EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY received FDA 510(k) clearance on 2000-12-28, under 510(k) number K001576.

Who is the listed applicant for EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY?

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

What is the FDA product code for EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY?

The FDA product code for EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY is NBV.

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Related Devices (Code: NBV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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