Cleared Traditional

K934011 - MITYVAC OBSTETRIC VAC DELIV KIT W/UNIV ...

K934011 is the FDA 510(k) clearance for MITYVAC OBSTETRIC VAC DELIV KIT W/UNIV ... by Neward Enterprises, Inc.. It is a Class 2 Obstetrics & Gynecology device (product code HDB) cleared through the Traditional 510(k) pathway after a 260-day FDA review.

K934011 · Neward Enterprises, Inc. · Obstetrics & Gynecology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1994
Decision
260d
Days
Class 2
Risk

K934011 is an FDA 510(k) clearance for the MITYVAC(R) OBSTETRIC VAC DELIV KIT W/UNIV VAC RELEASE. Classified as Extractor, Vacuum, Fetal (product code HDB), Class II - Special Controls.

Submitted by Neward Enterprises, Inc. (Cucamonga, US). The FDA issued a Cleared decision on May 4, 1994 after a review of 260 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.4340 - 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 Neward Enterprises, Inc. devices

Submission Details

510(k) Number K934011 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 17, 1993
Decision Date May 04, 1994
Days to Decision 260 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
100d slower than avg
Panel avg: 160d · This submission: 260d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code HDB Extractor, Vacuum, Fetal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.4340
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.

Regulatory Peers - HDB Extractor, Vacuum, Fetal

Devices cleared under the same product code (HDB) and FDA review panel - the closest regulatory comparables to K934011.
Kiwi® Complete Vacuum Delivery System, OmniCup® (VAC-DUAL M)
K250298 · Clinical Innovations, LLC · Oct 2025
MEDELA SINGLE USE SILC CUP, MODEL 077.0791
K041579 · Medela AG · Apr 2005
AMEDA DISPOSABLE VACUUM ASSIST CUP WITH FLUID RETENTION TRAP
K980976 · Hollister, Inc. · Aug 1998
AMEDA/EGNELL DOLPHIN DISPO-SOFT VACUUM EXTRACTOR
K895700 · Hollister, Inc. · Apr 1990
SILASTIC BRAND OBSTETRICAL VACUUM CUP
K771558 · Dow Corning Corp. Healthcare Industries Materials · Sep 1977