Cleared Traditional

K896885 - DISPOSABLE RESPIRTORY KIT (MP-200)

K896885 is an FDA 510(k) clearance for DISPOSABLE RESPIRTORY KIT (MP-200), manufactured by Medipart Jerry Alexander. The device is a Class 2 Radiology device with product code IYT cleared through the Traditional 510(k) pathway after a 80-day FDA review.

K896885 · Medipart Jerry Alexander · Radiology device
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Feb 1990
Decision
80d
Days
Class 2
Risk

K896885 is an FDA 510(k) clearance for the DISPOSABLE RESPIRTORY KIT (MP-200). Classified as System, Rebreathing, Radionuclide (product code IYT), Class II - Special Controls.

Submitted by Medipart Jerry Alexander (Cary, US). The FDA issued a Cleared decision on February 26, 1990 after a review of 80 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1390 - the FDA radiology and imaging software 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 Medipart Jerry Alexander devices

FDA 510(k) Submission Details - K896885

510(k) Number K896885 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 08, 1989
Decision Date February 26, 1990
Days to Decision 80 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
27d faster than avg
Panel avg: 107d · This submission: 80d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYT Device Classification - Class 2, Special Controls

Product Code IYT System, Rebreathing, Radionuclide
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1390
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 Radiology devices follow this clearance model.

Regulatory Peers - IYT System, Rebreathing, Radionuclide

All 29
Devices cleared under the same product code (IYT) and FDA review panel - the closest regulatory comparables to K896885.
Patient Administration Set
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XENON GAS BREATHING CIRCUIT
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BOLUS XENON CIRCUIT
K912626 · Vital Signs, Inc. · Aug 1991
MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133M
K896125 · Medipart Jerry Alexander · Feb 1990
MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133
K896124 · Medipart Jerry Alexander · Jan 1990
DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELD
K896475 · Medipart Jerry Alexander · Jan 1990