Cleared Traditional

K930494 - PANOJECT MINIFUSOR MODEL 100 AMBULATORY INFUSION

K930494 is an FDA 510(k) clearance for PANOJECT MINIFUSOR MODEL 100 AMBULATORY..., manufactured by Elan Medical Technologies, Ltd.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 449-day FDA review.

K930494 · Elan Medical Technologies, Ltd. · General Hospital
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Apr 1994
Decision
449d
Days
Class 2
Risk

K930494 is an FDA 510(k) clearance for the PANOJECT MINIFUSOR MODEL 100 AMBULATORY INFUSION. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Elan Medical Technologies, Ltd. (Gainesville, US). The FDA issued a Cleared decision on April 26, 1994 after a review of 449 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5725 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind General Hospital submissions.

View all Elan Medical Technologies, Ltd. devices

FDA 510(k) Submission Details - K930494

510(k) Number K930494 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 01, 1993
Decision Date April 26, 1994
Days to Decision 449 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
320d slower than avg
Panel avg: 129d · This submission: 449d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FRN Device Classification - Class 2, Special Controls

Product Code FRN Pump, Infusion
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5725
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 - FRN Pump, Infusion

All 612
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