Cleared Traditional

K884786 - EAR IRRIGATION SET 101 (EARIGATOR)

K884786 is an FDA 510(k) clearance for EAR IRRIGATION SET 101 (EARIGATOR), manufactured by Physicians Supply Co.. The device is a Class 1 General Hospital device with product code KYZ cleared through the Traditional 510(k) pathway after a 162-day FDA review.

K884786 · Physicians Supply Co. · General Hospital
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Apr 1989
Decision
162d
Days
Class 1
Risk

K884786 is an FDA 510(k) clearance for the EAR IRRIGATION SET 101 (EARIGATOR). Classified as Syringe, Irrigating (non Dental) (product code KYZ), Class I - General Controls.

Submitted by Physicians Supply Co. (Sandy, US). The FDA issued a Cleared decision on April 26, 1989 after a review of 162 days - an extended review cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6960 - 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.

View all Physicians Supply Co. devices

FDA 510(k) Submission Details - K884786

510(k) Number K884786 FDA.gov
FDA Decision Cleared Substantially Equivalent - Direct De Novo (SESD)
Date Received November 15, 1988
Decision Date April 26, 1989
Days to Decision 162 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
33d slower than avg
Panel avg: 129d · This submission: 162d
Pathway characteristics
Predicate-based equivalence.

KYZ Device Classification - Class 1, General Controls

Product Code KYZ Syringe, Irrigating (non Dental)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 880.6960
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - KYZ Syringe, Irrigating (non Dental)

All 26
Devices cleared under the same product code (KYZ) and FDA review panel - the closest regulatory comparables to K884786.
IRRIGATION TRAY
K896800 · Westmark, Sterile Packing Systems, Inc. (Sps) · May 1990
STRYKER TRAUMA TRAY
K894470 · Stryker Corp. · Aug 1989
STERILE IRRIGATION TRAYS
K890728 · Cypress Medical Products, Ltd. · Jun 1989
SURGICAL SEALANT APPLICATOR
K883338 · Micromedics, Inc. · Aug 1988
SURGICAL SEALANT DISPENSER (SSD)
K881020 · Micromedics, Inc. · Mar 1988
CLEAN-FLUSH
K830572 · Burron Medical Products, Inc. · Mar 1983