Cleared Traditional

K850277 - VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.

K850277 is an FDA 510(k) clearance for VIGGO I.V. ACCESSORIES-VIGGO EXTENSION ..., manufactured by Viggo Products. The device is a Class 2 General Hospital device with product code FPA cleared through the Traditional 510(k) pathway after a 79-day FDA review.

K850277 · Viggo Products · General Hospital
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Apr 1985
Decision
79d
Days
Class 2
Risk

K850277 is an FDA 510(k) clearance for the VIGGO I.V. ACCESSORIES-VIGGO EXTENSION TUBES ETC.. Classified as Set, Administration, Intravascular (product code FPA), Class II - Special Controls.

Submitted by Viggo Products (Madison, US). The FDA issued a Cleared decision on April 12, 1985 after a review of 79 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 Viggo Products devices

FDA 510(k) Submission Details - K850277

510(k) Number K850277 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 23, 1985
Decision Date April 12, 1985
Days to Decision 79 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
50d faster than avg
Panel avg: 129d · This submission: 79d
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 855
Devices cleared under the same product code (FPA) and FDA review panel - the closest regulatory comparables to K850277.
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K852488 · Y · Jun 1985
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K852140 · North American Instrument Corp. · May 1985
CORRECT FLO
K851299 · Norton Performance Plastics Corp. · May 1985
IVAC DRUG ADMINISTRATION DEVICE
K844843 · Y · Apr 1985
MICRO VOLUME DOUBLE LINE EXTENSION SET
K850061 · Travenol Laboratories, S.A. · Mar 1985
CRITIKON I.V. ADMINISTRAION SET
K850507 · Critikon Company, LLC · Mar 1985