Cleared Traditional

K883260 - DITTMAR POWER LIFTER

K883260 is an FDA 510(k) clearance for DITTMAR POWER LIFTER, manufactured by Dittmar and Penn Corp.. The device is a Class 1 General Hospital device with product code FOX cleared through the Traditional 510(k) pathway after a 96-day FDA review.

K883260 · Dittmar and Penn Corp. · General Hospital
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Nov 1988
Decision
96d
Days
Class 1
Risk

K883260 is an FDA 510(k) clearance for the DITTMAR POWER LIFTER. Classified as Stand, Infusion (product code FOX), Class I - General Controls.

Submitted by Dittmar and Penn Corp. (Cheltenham, US). The FDA issued a Cleared decision on November 7, 1988 after a review of 96 days - within the typical 510(k) review window.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6990 - 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. Standard predicate reliance. 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 Dittmar and Penn Corp. devices

FDA 510(k) Submission Details - K883260

510(k) Number K883260 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 03, 1988
Decision Date November 07, 1988
Days to Decision 96 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
33d faster than avg
Panel avg: 129d · This submission: 96d
Pathway characteristics
Predicate-based equivalence.

FOX Device Classification - Class 1, General Controls

Product Code FOX Stand, Infusion
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6990
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 - FOX Stand, Infusion

All 11
Devices cleared under the same product code (FOX) and FDA review panel - the closest regulatory comparables to K883260.
STAND, INFUSION
K946201 · Medical Specialties, Inc. · Apr 1995
FLEXSYS MOBILEMATE EQUIPMENT STAND
K944580 · Hill-Rom, Inc. · Mar 1995
HANGER, INTRAVENOUS/I.V. BAG HANGER OR HOLDER
K883133 · Ferguson Medical · Nov 1988
POLE, INTRAVENOUS
K880537 · Ferguson Medical · Apr 1988
TRACK AND CARRIER, INTRAVENOUS
K880538 · Ferguson Medical · Feb 1988
IMPACT 901 SERIES PORT-A-WALL
K850671 · Impact Instrumentation, Inc. · Mar 1985