Cleared Traditional

K072482 - HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY

K072482 is an FDA 510(k) clearance for HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY, manufactured by Smiths Medical Asd, Inc.. The device is a Class 2 General Hospital device with product code MEG cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K072482 · Smiths Medical Asd, Inc. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2007
Decision
86d
Days
Class 2
Risk

K072482 is an FDA 510(k) clearance for the HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY. Classified as Syringe, Antistick (product code MEG), Class II - Special Controls.

Submitted by Smiths Medical Asd, Inc. (Keene, US). The FDA issued a Cleared decision on November 29, 2007 after a review of 86 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.

FDA 510(k) Submission Details - K072482

510(k) Number K072482 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 04, 2007
Decision Date November 29, 2007
Days to Decision 86 days
Submission Type Traditional
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 129d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MEG Device Classification - Class 2, Special Controls

Product Code MEG Syringe, Antistick
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 - MEG Syringe, Antistick

All 162
Devices cleared under the same product code (MEG) and FDA review panel - the closest regulatory comparables to K072482.
ULTIMED ULTICARE SAFETY SYRINGE
K080600 · Ultimed, Inc. · Jun 2008
JIERUI SYRINGES AND NEEDLES
K072739 · Shandong Weigao Group Medical Polymer Co., Ltd. · Mar 2008
NEEDLE-TRAP/NEEDLE SAFETY LABEL
K073206 · Schreiner Medipharm · Jan 2008
CAREO SAFETY SYRINGE FOR U-100 INSULIN 0.5CC/ML
K072037 · Life-Shield Products, Inc. · Aug 2007
SSAFE PLUS DISPOSABLE SAFETY SYRINGE, 3 CC AND 5 CC
K070117 · Dolomite Biotech Sdn Bhd · Aug 2007
INVIROSNAP SAFETY SYRINGE, MODELS 120006, 120007, 120008, 100080, 130022, 130023 AND 130024
K070203 · Inviro Medical Devices, Inc. · Apr 2007
K072482 · HYPODERMIC NEEDLE-PRO SAFETY ALLERGY TRAY
Download PDF FDA Summary Smiths Medical Asd, I…