Cleared Traditional

K874360 - PLASTIC TUBING CONNECTOR

K874360 is an FDA 510(k) clearance for PLASTIC TUBING CONNECTOR, manufactured by American Medical Technology, Inc.. The device is a Class 2 General Hospital device with product code FPK cleared through the Traditional 510(k) pathway after a 25-day FDA review.

K874360 · American Medical Technology, Inc. · General Hospital
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Nov 1987
Decision
25d
Days
Class 2
Risk

K874360 is an FDA 510(k) clearance for the PLASTIC TUBING CONNECTOR. Classified as Tubing, Fluid Delivery (product code FPK), Class II - Special Controls.

Submitted by American Medical Technology, Inc. (Brooklyn, US). The FDA issued a Cleared decision on November 17, 1987 after a review of 25 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 American Medical Technology, Inc. devices

FDA 510(k) Submission Details - K874360

510(k) Number K874360 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 23, 1987
Decision Date November 17, 1987
Days to Decision 25 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
104d faster than avg
Panel avg: 129d · This submission: 25d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FPK Device Classification - Class 2, Special Controls

Product Code FPK Tubing, Fluid Delivery
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 - FPK Tubing, Fluid Delivery

All 30
Devices cleared under the same product code (FPK) and FDA review panel - the closest regulatory comparables to K874360.
HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET
K884156 · Sechrist Industries, Inc. · Nov 1988
IV EXTENSION SET
K875186 · Marquette Medical, Inc. · Feb 1988
INFUSION MANIFOLD
K873852 · Advanced Surgical Products, Inc. · Nov 1987
EXTENSION TUBE PUMP SET
K871085 · Churchill Corp. · Jun 1987
CHURCHILL EXTENSION TUBE
K861626 · Churchill Corp. · Jun 1986
CHURCHILL-H EXTENSION TUBE
K854629 · Churchill Corp. · Dec 1985