Cleared Traditional

K861152 - EXEL VACUUM BLOOD COLLECTING SYSTEM

K861152 is the FDA 510(k) clearance for EXEL VACUUM BLOOD COLLECTING SYSTEM by Exel Intl.. It is a Class 2 General Hospital device (product code FMI) cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K861152 · Exel Intl. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1986
Decision
41d
Days
Class 2
Risk

K861152 is an FDA 510(k) clearance for the EXEL VACUUM BLOOD COLLECTING SYSTEM. Classified as Needle, Hypodermic, Single Lumen (product code FMI), Class II - Special Controls.

Submitted by Exel Intl. (Culver City, US). The FDA issued a Cleared decision on May 6, 1986 after a review of 41 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.5570 - 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 Exel Intl. devices

Submission Details

510(k) Number K861152 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 26, 1986
Decision Date May 06, 1986
Days to Decision 41 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
88d faster than avg
Panel avg: 129d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code FMI Needle, Hypodermic, Single Lumen
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.5570
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 - FMI Needle, Hypodermic, Single Lumen

All 237
Devices cleared under the same product code (FMI) and FDA review panel - the closest regulatory comparables to K861152.
ULTRA-VUE SPINAL TYPE BIOPSY NEEDLE
K862610 · Bd Becton Dickinson Vacutainer Systems Preanalytic · Feb 1987
DEPTH MEASURING NEEDLES/VASCU IMPLANT ACCESS SET
K861390 · Baxter Healthcare Corp · Jul 1986
ICU MEDICAL NEEDLE, LOPEZ NEEDLE
K860781 · Icu Medical, Inc. · May 1986
DISPOSABLE NEEDLE COUNTER (20-720)
K861318 · Anago, Inc. · May 1986
BLOOD COLLECTING NEEDLE
K855248 · Churchill Corp. · Feb 1986
MONOJECT STERILE M200 ALUMINUM/M250 POLYPROPYLENE
K854547 · Sherwood Medical Co. · Feb 1986