Cleared Traditional

K945548 - MEDIVAX

K945548 is an FDA 510(k) clearance for MEDIVAX, manufactured by Vitajet Corp.. The device is a Class 2 General Hospital device with product code KZE cleared through the Traditional 510(k) pathway after a 371-day FDA review.

K945548 · Vitajet Corp. · General Hospital
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Nov 1995
Decision
371d
Days
Class 2
Risk

K945548 is an FDA 510(k) clearance for the MEDIVAX. Classified as Injector, Fluid, Non-electrically Powered (product code KZE), Class II - Special Controls.

Submitted by Vitajet Corp. (Laguna Hills, US). The FDA issued a Cleared decision on November 20, 1995 after a review of 371 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5430 - the FDA general hospital 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. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

View all Vitajet Corp. devices

FDA 510(k) Submission Details - K945548

510(k) Number K945548 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1994
Decision Date November 20, 1995
Days to Decision 371 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
242d slower than avg
Panel avg: 129d · This submission: 371d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KZE Device Classification - Class 2, Special Controls

Product Code KZE Injector, Fluid, Non-electrically Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5430
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 General Hospital devices follow this clearance model.

Regulatory Peers - KZE Injector, Fluid, Non-electrically Powered

All 11
Devices cleared under the same product code (KZE) and FDA review panel - the closest regulatory comparables to K945548.
VITAJET
K962625 · Vitajet Corp. · Dec 1996
MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM
K962956 · Medi-Ject Corp. · Oct 1996
MEDI-JECT CORPORATION MEDI-JECTOR NEEDLE-FREE BIO-TROPIN DDRUG DELIVERY SYSTEMS 0.0058/0.0068(INCH DIAMETER NOZZLEORIFIC
K960285 · Medi-Ject Corp. · Apr 1996
PRECI-JET 50
K851181 · Ulster Scientific, Inc. · Jun 1985