Cleared Traditional

K934206 - MAVIG ANGIO SHIELD MODELS 6290 & 6272

K934206 is an FDA 510(k) clearance for MAVIG ANGIO SHIELD MODELS 6290 & 6272, manufactured by F. Walter Hanel GmbH. The device is a Class 1 Radiology device with product code KPY cleared through the Traditional 510(k) pathway after a 38-day FDA review.

K934206 · F. Walter Hanel GmbH · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1993
Decision
38d
Days
Class 1
Risk

K934206 is an FDA 510(k) clearance for the MAVIG ANGIO SHIELD MODELS 6290 & 6272. Classified as Shield, Protective, Personnel (product code KPY), Class I - General Controls.

Submitted by F. Walter Hanel GmbH (North Attleboro, US). The FDA issued a Cleared decision on October 7, 1993 after a review of 38 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.6500 - the FDA radiology and imaging software oversight 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 F. Walter Hanel GmbH devices

FDA 510(k) Submission Details - K934206

510(k) Number K934206 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 1993
Decision Date October 07, 1993
Days to Decision 38 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 107d · This submission: 38d
Pathway characteristics
Predicate-based equivalence.

KPY Device Classification - Class 1, General Controls

Product Code KPY Shield, Protective, Personnel
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 892.6500
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KPY Shield, Protective, Personnel

All 7
Devices cleared under the same product code (KPY) and FDA review panel - the closest regulatory comparables to K934206.
INTRA-ORAL THERMOPLASTIC SHIELD
K962622 · Medtec, Inc. · Oct 1996
THERMOPLASTIC SHIELD
K954456 · Medtec, Inc. · Dec 1995
UTK-DTE AUTILARY SHIELD
K954146 · Mallinckrodt Medical · Dec 1995
DU PONT XENOLITE(TM) RADIATION PROTECTION APPAREL
K896511 · E.I. Dupont DE Nemours & Co., Inc. · Dec 1989
VENTIBOX
K844160 · Syncor Intl. Corp. · Dec 1984
BYPASS COIL
K811068 · G.D. Searle and Co. · May 1981