Cleared Traditional

K830901 - CONNECTOR 5 IN 1, T-CONNECTOR

K830901 is an FDA 510(k) clearance for CONNECTOR 5 IN 1, manufactured by Medical Specialists IN Packaging. The device is a Class 2 General Hospital device with product code GAZ cleared through the Traditional 510(k) pathway after a 16-day FDA review.

K830901 · Medical Specialists IN Packaging · General Hospital
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Apr 1983
Decision
16d
Days
Class 2
Risk

K830901 is an FDA 510(k) clearance for the CONNECTOR 5 IN 1, T-CONNECTOR. Classified as Tubing, Noninvasive (product code GAZ), Class II - Special Controls.

Submitted by Medical Specialists IN Packaging (Mchenry, US). The FDA issued a Cleared decision on April 6, 1983 after a review of 16 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6740 - 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 Specialists IN Packaging devices

FDA 510(k) Submission Details - K830901

510(k) Number K830901 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 21, 1983
Decision Date April 06, 1983
Days to Decision 16 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
113d faster than avg
Panel avg: 129d · This submission: 16d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAZ Device Classification - Class 2, Special Controls

Product Code GAZ Tubing, Noninvasive
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6740
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 - GAZ Tubing, Noninvasive

All 16
Devices cleared under the same product code (GAZ) and FDA review panel - the closest regulatory comparables to K830901.
5 - IN - 1 CONNECTOR
K864964 · Medovations, Inc. · Jan 1987
PHARMA-PLAST SMOOTH BORE CONNECTORS
K843476 · Zimmar Consulting , Ltd. · Sep 1984
STERILE 5 IN 1 CONNECTORS
K830835 · Abco Dealers, Inc. · Apr 1983
STERILE SAFETY PINS
K830381 · Devon Industries, Inc. · Mar 1983
PLEUROFIX THORACENTESIS KIT
K820004 · Burron Medical Products, Inc. · Feb 1982
ARGYLE CONNECT TUBE-CON & NON
K802777 · Sherwood Medical Co. · Dec 1980