Cleared Traditional

K870330 - SP55 SYRINGE PUMP

K870330 is an FDA 510(k) clearance for SP55 SYRINGE PUMP, manufactured by Vickers , Ltd.. The device is a Class 2 General Hospital device with product code FRN cleared through the Traditional 510(k) pathway after a 138-day FDA review.

K870330 · Vickers , Ltd. · General Hospital
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Jun 1987
Decision
138d
Days
Class 2
Risk

K870330 is an FDA 510(k) clearance for the SP55 SYRINGE PUMP. Classified as Pump, Infusion (product code FRN), Class II - Special Controls.

Submitted by Vickers , Ltd. (England, GB). The FDA issued a Cleared decision on June 15, 1987 after a review of 138 days - within the typical 510(k) review window.

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: 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 Vickers , Ltd. devices

FDA 510(k) Submission Details - K870330

510(k) Number K870330 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 28, 1987
Decision Date June 15, 1987
Days to Decision 138 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
9d slower than avg
Panel avg: 129d · This submission: 138d
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 618
Devices cleared under the same product code (FRN) and FDA review panel - the closest regulatory comparables to K870330.
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IMED(R) MODEL 965A VOLUMETRIC INFUSION PUMP
K870992 · Imed Corp. · Jun 1987
AMBULATORY INFUSION PUMP DRUG RESERVOIR
K870524 · Med Fusion Systems, Inc. · May 1987