Cleared Traditional

K800880 - PLASTIC TUBING ADAPTERS 5-IN-1-

K800880 is the FDA 510(k) clearance for PLASTIC TUBING ADAPTERS 5-IN-1- by Harvard Laboratories. It is a Class 2 Cardiovascular device (product code DTL) cleared through the Traditional 510(k) pathway after a 27-day FDA review.

K800880 · Harvard Laboratories · Cardiovascular device
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May 1980
Decision
27d
Days
Class 2
Risk

K800880 is an FDA 510(k) clearance for the PLASTIC TUBING ADAPTERS 5-IN-1-. Classified as Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass (product code DTL), Class II - Special Controls.

Submitted by Harvard Laboratories (Mchenry, US). The FDA issued a Cleared decision on May 14, 1980 after a review of 27 days - a notably fast clearance cycle.

This device falls under the Cardiovascular FDA review panel, regulated under 21 CFR 870.4290 - the FDA cardiovascular device oversight 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 Harvard Laboratories devices

Submission Details

510(k) Number K800880 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 17, 1980
Decision Date May 14, 1980
Days to Decision 27 days
Submission Type Traditional
Review Panel Cardiovascular (CV)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
98d faster than avg
Panel avg: 125d · This submission: 27d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.4290
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 Cardiovascular devices follow this clearance model.

Regulatory Peers - DTL Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

All 45
Devices cleared under the same product code (DTL) and FDA review panel - the closest regulatory comparables to K800880.
SCI MED TUBING CONNECTORS
K831261 · Scimed Life Systems, Inc. · Jun 1983
WM. HARVEY OVERPRESSURE SAFETY VALVE
K820297 · C.R. Bard, Inc. · Mar 1982
SAMPLING MANIFOLD H530
K801200 · C.R. Bard, Inc. · Jun 1980
CONPHAR MANOMETER CONNECTORS
K792113 · Conphar, Inc. · Dec 1979
3-WAY STOPCOCK W/MALE LOCKING LUER ADA.
K791914 · Abbott Laboratories · Oct 1979
MODIFIED STERILE DISPOSABLE STOPCOCKS
K781579 · Cobe Laboratories, Inc. · Oct 1978