Cleared Traditional

K870018 - E-Z JECT INSULIN SYRINGE

K870018 is an FDA 510(k) clearance for E-Z JECT INSULIN SYRINGE, manufactured by Can-Am Surgical Corp.. The device is a Class 2 General Hospital device with product code FMF cleared through the Traditional 510(k) pathway after a 33-day FDA review.

K870018 · Can-Am Surgical Corp. · General Hospital
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1987
Decision
33d
Days
Class 2
Risk

K870018 is an FDA 510(k) clearance for the E-Z JECT INSULIN SYRINGE. Classified as Syringe, Piston (product code FMF), Class II - Special Controls.

Submitted by Can-Am Surgical Corp. (Simi Valley, US). The FDA issued a Cleared decision on February 4, 1987 after a review of 33 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 Can-Am Surgical Corp. devices

FDA 510(k) Submission Details - K870018

510(k) Number K870018 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 02, 1987
Decision Date February 04, 1987
Days to Decision 33 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
96d faster than avg
Panel avg: 129d · This submission: 33d
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 523
Devices cleared under the same product code (FMF) and FDA review panel - the closest regulatory comparables to K870018.
MONOJECT PHARMACY TRAY
K860688 · Sherwood Medical Co. · Aug 1987
SURGITEK PHYSICIAN DISPEN. PATIENT SELF-INJECT KIT
K870518 · Surgitek · Apr 1987
ACCUPEN(R)
K870078 · Ulster Scientific, Inc. · Mar 1987
REFILLABLE SYRINGE
K864407 · Med Fusion Systems, Inc. · Jan 1987
VARIOUS SYRINGES W/NEEDLES, W/OUT NEEDLES, NEEDLES
K864747 · Jms Co., Ltd. · Dec 1986
USI AUTOJECT INSULIN SYRINGE
K864761 · Ulster Scientific, Inc. · Dec 1986