Cleared Traditional

K890082 - DISPENSING PIN/CHEMOTHERAPY DISPENSING PIN

K890082 is an FDA 510(k) clearance for DISPENSING PIN/CHEMOTHERAPY DISPENSING PIN, manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 21-day FDA review.

K890082 · Bd Becton Dickinson Vacutainer Systems Preanalytic · General Hospital
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Jan 1989
Decision
21d
Days
Class 2
Risk

K890082 is an FDA 510(k) clearance for the DISPENSING PIN/CHEMOTHERAPY DISPENSING PIN. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Franklin Lakes, US). The FDA issued a Cleared decision on January 31, 1989 after a review of 21 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 Bd Becton Dickinson Vacutainer Systems Preanalytic devices

FDA 510(k) Submission Details - K890082

510(k) Number K890082 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 10, 1989
Decision Date January 31, 1989
Days to Decision 21 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
108d faster than avg
Panel avg: 129d · This submission: 21d
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 524
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K890082.
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MODEL #535 PACU STRETCHER/BED & #530 ED/TRAUMA STR
K894335 · Midmark Corp. · Sep 1989
CONTROL SYRINGE
K884497 · Professional Medical Services · Dec 1988
SINGLE-FIL(TM) SYRINGE
K883955 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Oct 1988
MANAN HUBER STYLE INFUSION NEEDLE
K883744 · Manan Medical Products, Inc. · Sep 1988