Cleared Traditional

K895419 - DISPOSABLE DISC FILTER

K895419 is an FDA 510(k) clearance for DISPOSABLE DISC FILTER, manufactured by The Medi-Dose Group. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K895419 · The Medi-Dose Group · General Hospital
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Nov 1989
Decision
84d
Days
Class 2
Risk

K895419 is an FDA 510(k) clearance for the DISPOSABLE DISC FILTER. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by The Medi-Dose Group (Feasterville, US). The FDA issued a Cleared decision on November 24, 1989 after a review of 84 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5860 - 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 The Medi-Dose Group devices

FDA 510(k) Submission Details - K895419

510(k) Number K895419 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 01, 1989
Decision Date November 24, 1989
Days to Decision 84 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
45d faster than avg
Panel avg: 129d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FMF Device Classification - Class 2, Special Controls

Product Code FMF Syringe, Piston
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5860
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 - FMF Syringe, Piston

All 535
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K895419.
JOHNSON & JOHNSON DUAL SYRINGE APPLICATOR
K902157 · Johnson & Johnson Medical, Inc. · Nov 1990
DISPOSABLE CORONARY CONTROL SYRINGE
K902346 · Advance Medical Designs, Inc. · Jun 1990
AUTOPEN
K895890 · Ulster Scientific, Inc. · Feb 1990
INTOPO
K894206 · Acacia, Inc. · Oct 1989
30-CS01, 30-CS02, 30-CS03 CONTROL SYRINGES
K894801 · Advance Medical Designs, Inc. · Sep 1989
NEEDLE*LESS DRUG VIAL ADAPTER
K894177 · Baxter Healthcare Corp · Sep 1989