Cleared Traditional

K061896 - MEDIAID DISPOSABLE NON-ADHESIVE SENSORS

Also marketed or referenced as:
REUSABLE FINGER CLIP SP02 SENSORS, MODEL CST060-2101N

K061896 is an FDA 510(k) clearance for MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, manufactured by Mediaid, Inc.. The device is a Class 2 Anesthesiology device with product code DQA cleared through the Traditional 510(k) pathway after a 283-day FDA review.

K061896 · Mediaid, Inc. · Anesthesiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 2007
Decision
283d
Days
Class 2
Risk

K061896 is an FDA 510(k) clearance for the MEDIAID DISPOSABLE NON-ADHESIVE SENSORS, MODEL CST050-2101N. Classified as Oximeter (product code DQA), Class II - Special Controls.

Submitted by Mediaid, Inc. (Cerritos, US). The FDA issued a Cleared decision on April 12, 2007 after a review of 283 days - an extended review cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 870.2700 - the FDA anesthesiology and respiratory 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 Anesthesiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Mediaid, Inc. devices

FDA 510(k) Submission Details - K061896

510(k) Number K061896 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 03, 2006
Decision Date April 12, 2007
Days to Decision 283 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
143d slower than avg
Panel avg: 140d · This submission: 283d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DQA Device Classification - Class 2, Special Controls

Product Code DQA Oximeter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 870.2700
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - DQA Oximeter

All 478
Devices cleared under the same product code (DQA) and FDA review panel - the closest regulatory comparables to K061896.
DURAMAX REUSABLE OXIMETRY SENSOR
K070408 · Nellcor Puritan Bennett, Inc. · May 2007
LIFESENSE, MODEL LS1-9R
K063752 · Nonin Medical, Inc. · May 2007
PHILIPS REUSABLE SPO2 SENSORS M1191T, M1192T AND M1193T, CLIP SENSOR M1196T AND DISPOSABLE SPO2 SENSORS M1131A, M1132A
K063783 · Philips Medical Systems, Inc. · Apr 2007
CADWELL EASYNET OXIMETER MODULE
K061706 · Cadwell Laboratories, Inc. · Mar 2007
RAINBOW ADHESIVE CO-OXIMETRY SENSORS
K063140 · Masimo Corporation · Dec 2006
PHILIPS SPO2 REUSABLE SENSOR, MODELS M1196A AND M1196T
K062605 · Philips Medical Systems · Nov 2006