Cleared Traditional

K853527 - JUFREY CORP. UNIV. DISPOS. SCALP VEIN I...

K853527 is the FDA 510(k) clearance for JUFREY CORP. UNIV. DISPOS. SCALP VEIN I... by Jufrey Multimed Corp.. It is a Class 2 General Hospital device (product code FPA) cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K853527 · Jufrey Multimed Corp. · General Hospital
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Sep 1985
Decision
46d
Days
Class 2
Risk

K853527 is an FDA 510(k) clearance for the JUFREY CORP. UNIV. DISPOS. SCALP VEIN INFUSION SET. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Jufrey Multimed Corp. (Washington, US). The FDA issued a Cleared decision on September 23, 1985 after a review of 46 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 Jufrey Multimed Corp. devices

Submission Details

510(k) Number K853527 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 08, 1985
Decision Date September 23, 1985
Days to Decision 46 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
83d faster than avg
Panel avg: 129d · This submission: 46d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FPA Set, Administration, Intravascular
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 - FPA Set, Administration, Intravascular

All 281
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