Cleared Traditional

K853075 - MEDNOVA SAFETY BAG

K853075 is an FDA 510(k) clearance for MEDNOVA SAFETY BAG, manufactured by Mednova Corp.. The device is a Class 2 General Hospital device with product code LHI cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K853075 · Mednova Corp. · General Hospital
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Oct 1985
Decision
85d
Days
Class 2
Risk

K853075 is an FDA 510(k) clearance for the MEDNOVA SAFETY BAG. Classified as Set, I.v. Fluid Transfer (product code LHI), Class II - Special Controls.

Submitted by Mednova Corp. (New York, US). The FDA issued a Cleared decision on October 16, 1985 after a review of 85 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Mednova Corp. devices

FDA 510(k) Submission Details - K853075

510(k) Number K853075 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 23, 1985
Decision Date October 16, 1985
Days to Decision 85 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
44d faster than avg
Panel avg: 129d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LHI Device Classification - Class 2, Special Controls

Product Code LHI Set, I.v. Fluid Transfer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - LHI Set, I.v. Fluid Transfer

All 145
Devices cleared under the same product code (LHI) and FDA review panel - the closest regulatory comparables to K853075.
MODIFIED HC-417 BAG TO BAG & HC-418 BOTTLE TO BAG
K861434 · Churchill Corp. · May 1986
SLIDING RECONSTITUTION DEVICE W/ADMIX VIALEX PLAST
K853830 · Travenol Laboratories, S.A. · Nov 1985
VIAL VENT FILTER
K852467 · Baxter Healthcare Corp · Oct 1985
FLOW EASE(PLASTIC VENTED NEEDLE)
K853212 · Acacia, Inc. · Sep 1985
TRANSFER DEVICE
K853188 · Advance Medical Designs, Inc. · Aug 1985
TANDEM SETS I.V.
K850757 · Acacia, Inc. · Apr 1985