Cleared Traditional

K980454 - LYSONIX ASPIRATION PUMP

K980454 is an FDA 510(k) clearance for LYSONIX ASPIRATION PUMP, manufactured by Lysonix, Inc.. The device is a Class 2 General & Plastic Surgery device with product code BTA cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K980454 · Lysonix, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1998
Decision
41d
Days
Class 2
Risk

K980454 is an FDA 510(k) clearance for the LYSONIX ASPIRATION PUMP. Classified as Pump, Portable, Aspiration (manual Or Powered) (product code BTA), Class II - Special Controls.

Submitted by Lysonix, Inc. (Carpinteria, US). The FDA issued a Cleared decision on March 18, 1998 after a review of 41 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4780 - the FDA general and plastic surgery 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 Lysonix, Inc. devices

FDA 510(k) Submission Details - K980454

510(k) Number K980454 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 05, 1998
Decision Date March 18, 1998
Days to Decision 41 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
74d faster than avg
Panel avg: 115d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTA Device Classification - Class 2, Special Controls

Product Code BTA Pump, Portable, Aspiration (manual Or Powered)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4780
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 & Plastic Surgery devices follow this clearance model.

Regulatory Peers - BTA Pump, Portable, Aspiration (manual Or Powered)

All 89
Devices cleared under the same product code (BTA) and FDA review panel - the closest regulatory comparables to K980454.
DEVILBISS MODEL 6305D HEAVY DUTY AC ASPIRATOR
K981602 · Sunrise Medical Hhg, Inc. · Jul 1998
EASYGO ASPIRATOR
K971749 · Precision Medical, Inc. · Apr 1998
IP-16
K980301 · Servizi Medico Estetici Italinai Srl. · Mar 1998
PSI-TEC ASPIRATOR
K980392 · Byron Medical · Mar 1998
MICROAIRE POWER ASPIRATION DEVICE PAD SYSTEM
K973268 · Microaire Surgical Instruments, Inc. · Nov 1997
ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER STR5
K971107 · Alexander Mfg. Co. · Jun 1997