Cleared Traditional

K873736 - NICOLET DIGITAL TWO PIECE HEARING AID

K873736 is the FDA 510(k) clearance for NICOLET DIGITAL TWO PIECE HEARING AID by Nicolet Biomedical Instruments. It is a Class 1 Ear, Nose, Throat device (product code ESD) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K873736 · Nicolet Biomedical Instruments · Ear, Nose, Throat device
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Dec 1987
Decision
84d
Days
Class 1
Risk

K873736 is an FDA 510(k) clearance for the NICOLET DIGITAL TWO PIECE HEARING AID. Classified as Hearing Aid, Air-conduction, Prescription (product code ESD), Class I - General Controls.

Submitted by Nicolet Biomedical Instruments (Madison, US). The FDA issued a Cleared decision on December 8, 1987 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Ear, Nose, Throat FDA review panel, regulated under 21 CFR 874.3300 - 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.

View all Nicolet Biomedical Instruments devices

Submission Details

510(k) Number K873736 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 15, 1987
Decision Date December 08, 1987
Days to Decision 84 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
5d faster than avg
Panel avg: 89d · This submission: 84d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code ESD Hearing Aid, Air-conduction, Prescription
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 874.3300
Definition An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid.
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 - ESD Hearing Aid, Air-conduction, Prescription

All 661
Devices cleared under the same product code (ESD) and FDA review panel - the closest regulatory comparables to K873736.
BTE HEARING AID OTICON MODEL E39PL
K874381 · Oticon Corp. · Dec 1987
POST AURICULAR HEARING AID 46PP-PC SUMMIT
K874707 · Richards Medical Co., Inc. · Dec 1987
OTICON MODEL I50 IN-THE-EAR HEARING AID
K874744 · Oticon Corp. · Dec 1987
U-IMPULSE TVC AIR CONDUCTION HEARING AID
K873559 · Richards Medical Co., Inc. · Oct 1987
CUSTOM IN-THE-EAR HEARING AID SERIES MCA20
K873468 · Maico Hearing Instruments, Inc. · Sep 1987
U-IMPULSE AIR CONDUCTION IN-THE-CANAL HEARING AID
K873560 · Richards Medical Co., Inc. · Sep 1987