Cleared Traditional

K983576 - DR180-R/OXY

K983576 is an FDA 510(k) clearance for DR180-R/OXY, manufactured by North East Monitoring, Inc.. The device is a Class 2 General Hospital device with product code FLL cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K983576 · North East Monitoring, Inc. · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Mar 1999
Decision
161d
Days
Class 2
Risk

K983576 is an FDA 510(k) clearance for the DR180-R/OXY. Classified as Continuous Measurement Thermometer (product code FLL), Class II - Special Controls.

Submitted by North East Monitoring, Inc. (Sudbury, US). The FDA issued a Cleared decision on March 23, 1999 after a review of 161 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.2910 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General Hospital review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K983576

510(k) Number K983576 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 1998
Decision Date March 23, 1999
Days to Decision 161 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
32d slower than avg
Panel avg: 129d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FLL Device Classification - Class 2, Special Controls

Product Code FLL Continuous Measurement Thermometer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.2910
Definition A Continuous Measurement Thermometer Is A Clinical Electronic Thermometer Indicated To Measure The Body Or Skin Temperature Of A Person Continuously Or In Specified Intervals. Under This Regulation, This Product Code Represents Non-exempt Devices. For More Information, See 90 Fr 25889, Available At Https://www.govinfo.gov/content/pkg/fr-2025-06-18/pdf/2025-11207.pdf.
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 - FLL Continuous Measurement Thermometer

All 663
Devices cleared under the same product code (FLL) and FDA review panel - the closest regulatory comparables to K983576.
DUTECK DIGITAL CLINICAL THERMOMETER
K992327 · Duteck Industrial Co., Ltd. · Aug 1999
SD-100 SKYEAR THERMOMETER
K984506 · Skylark Device Co., Ltd. · Jul 1999
TEMP TELLER-INFRARED TYMPANIC THERMOMETER, MODELS TT-200, TT-201
K984497 · Oriental System Technology, Inc. · May 1999
BRAUN THERMOSCAN IRT3020/3500 ONE SECONS EAR THERMOMETER, MODEL IRT3020/3520
K983295 · Braun AG · Mar 1999
SABRATEK APM-2000 AMBULATORY PATIENT MONTOR, TRANSCUTANEOUS TEMPERATURE MONITOR
K983355 · Sabratek Corp. · Mar 1999
MICROLIFE IT2CA1
K990168 · Microlife Systems AG · Feb 1999