Cleared Traditional

K001576 - EVA -VACUUM ASSIST DEVICE FOR CLITORAL ...

K001576 is an FDA 510(k) clearance for EVA -VACUUM ASSIST DEVICE FOR CLITORAL ..., manufactured by Prosurg, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code NBV cleared through the Traditional 510(k) pathway after a 220-day FDA review.

K001576 · Prosurg, Inc. · Obstetrics & Gynecology device
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Dec 2000
Decision
220d
Days
Class 2
Risk

K001576 is an FDA 510(k) clearance for the EVA -VACUUM ASSIST DEVICE FOR CLITORAL THERAPY. Classified as Device, Engorgement, Clitoral (product code NBV), Class II - Special Controls.

Submitted by Prosurg, Inc. (San Jose, US). The FDA issued a Cleared decision on December 28, 2000 after a review of 220 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5970 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Prosurg, Inc. devices

FDA 510(k) Submission Details - K001576

510(k) Number K001576 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 22, 2000
Decision Date December 28, 2000
Days to Decision 220 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
60d slower than avg
Panel avg: 160d · This submission: 220d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NBV Device Classification - Class 2, Special Controls

Product Code NBV Device, Engorgement, Clitoral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5970
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.