Cleared Traditional

K882744 - EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM

K882744 is an FDA 510(k) clearance for EFFNER ILLUMINATED NASAL TRACHEOSTOMA S..., manufactured by Effner, Inc.. The device is a Class 2 Ear, Nose, Throat device with product code EOB cleared through the Traditional 510(k) pathway after a 40-day FDA review.

K882744 · Effner, Inc. · Ear, Nose, Throat device
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Optimized for regulatory review, auditing and printing
Aug 1988
Decision
40d
Days
Class 2
Risk

K882744 is an FDA 510(k) clearance for the EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM. Classified as Nasopharyngoscope (flexible Or Rigid) (product code EOB), Class II - Special Controls.

Submitted by Effner, Inc. (Port Washington, US). The FDA issued a Cleared decision on August 10, 1988 after a review of 40 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.4760 - the FDA ear, nose and throat 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 - K882744

510(k) Number K882744 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1988
Decision Date August 10, 1988
Days to Decision 40 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
50d faster than avg
Panel avg: 90d · This submission: 40d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EOB Device Classification - Class 2, Special Controls

Product Code EOB Nasopharyngoscope (flexible Or Rigid)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.4760
Definition If The Device Is Reusable, Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.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 Ear, Nose, Throat devices follow this clearance model.

Regulatory Peers - EOB Nasopharyngoscope (flexible Or Rigid)

All 158
Devices cleared under the same product code (EOB) and FDA review panel - the closest regulatory comparables to K882744.
PENTAX NASO-PHARYNGO-LARYNGOSCOPE FNL-15P2/15RP2
K921707 · Pentax Precision Instrument Corp. · Jul 1992
FLEXIBLE NASOPHARYNGOSCOPE
K896297 · Jedmed Instrument Co. · Jan 1990
FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE
K895245 · Optimed Technologies, Inc. · Nov 1989
ENDOSCOPES FOR SINUS SURGERY
K874215 · Richards Medical Co., Inc. · Jan 1988
K882744 · EFFNER ILLUMINATED NASAL TRACHEOSTOMA SPECULUM
Download PDF Effner, Inc.