Cleared Traditional

K821764 - DISPOSABLE INTRAVENOUS INJECTION SYSTEM

K821764 is an FDA 510(k) clearance for DISPOSABLE INTRAVENOUS INJECTION SYSTEM, manufactured by Medical Systems Research. The device is a Class 2 General Hospital device with product code FPA cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K821764 · Medical Systems Research · General Hospital
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Jun 1982
Decision
20d
Days
Class 2
Risk

K821764 is an FDA 510(k) clearance for the DISPOSABLE INTRAVENOUS INJECTION SYSTEM. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Medical Systems Research (Mchenry, US). The FDA issued a Cleared decision on June 29, 1982 after a review of 20 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5440 - 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 Medical Systems Research devices

FDA 510(k) Submission Details - K821764

510(k) Number K821764 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 09, 1982
Decision Date June 29, 1982
Days to Decision 20 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
109d faster than avg
Panel avg: 129d · This submission: 20d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPA Device Classification - Class 2, Special Controls

Product Code FPA Set, Administration, Intravascular
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5440
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 - FPA Set, Administration, Intravascular

All 859
Devices cleared under the same product code (FPA) and FDA review panel - the closest regulatory comparables to K821764.
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K820747 · Sherwood Medical Co. · Apr 1982