Cleared Traditional

K782167 - DELTA FLOW

K782167 is the FDA 510(k) clearance for DELTA FLOW by Medex, Inc.. It is a Class 2 General Hospital device (product code FMG) cleared through the Traditional 510(k) pathway after a 54-day FDA review.

K782167 · Medex, Inc. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1979
Decision
54d
Days
Class 2
Risk

K782167 is an FDA 510(k) clearance for the DELTA FLOW. Classified as Stopcock, I.v. Set (product code FMG), Class II - Special Controls.

Submitted by Medex, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 21, 1979 after a review of 54 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 Medex, Inc. devices

Submission Details

510(k) Number K782167 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 29, 1978
Decision Date February 21, 1979
Days to Decision 54 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
75d faster than avg
Panel avg: 129d · This submission: 54d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FMG Stopcock, I.v. Set
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 - FMG Stopcock, I.v. Set

All 37
Devices cleared under the same product code (FMG) and FDA review panel - the closest regulatory comparables to K782167.
ARTERIOGRAM TRAY
K812927 · American Pharmaseal Div. Ahsc · Nov 1981
THREE-WAY STOPCOCK EXTENSION SET 20-SL
K800284 · Abbott Laboratories · Feb 1980
3-WAY STOPCOCK
K782168 · Medex, Inc. · Feb 1979
MANIFOLD, DISPOSABLE 3 VALVE
K790010 · Cordis Corp. · Feb 1979
SUPPLEMENTAL TYGON PAC-MONITORING LINES
K780662 · Norton Performance Plastics Corp. · Jun 1978
STOPCOCK
K780596 · Abco Dealers, Inc. · Apr 1978