Cleared Traditional

K884016 - DC-1 I.V. DOSAGE COMPUTER

K884016 is an FDA 510(k) clearance for DC-1 I.V. DOSAGE COMPUTER, manufactured by Phase Medical, Inc.. The device is a Class 2 General Hospital device with product code NDC cleared through the Traditional 510(k) pathway after a 89-day FDA review.

K884016 · Phase Medical, Inc. · General Hospital
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Dec 1988
Decision
89d
Days
Class 2
Risk

K884016 is an FDA 510(k) clearance for the DC-1 I.V. DOSAGE COMPUTER. Classified as Calculator, Drug Dose (product code NDC), Class II - Special Controls.

Submitted by Phase Medical, Inc. (Santa Ana, US). The FDA issued a Cleared decision on December 20, 1988 after a review of 89 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 868.1890 - 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 Phase Medical, Inc. devices

FDA 510(k) Submission Details - K884016

510(k) Number K884016 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 22, 1988
Decision Date December 20, 1988
Days to Decision 89 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
40d faster than avg
Panel avg: 129d · This submission: 89d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

NDC Device Classification - Class 2, Special Controls

Product Code NDC Calculator, Drug Dose
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 868.1890
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.