KCP · Syringe, Ent

Ear, Nose, Throat · 21 CFR 874.5220 · Class 1

Overview

Product CodeKCP
Device NameSyringe, Ent
Regulation21 CFR 874.5220
Device ClassClass 1
Review PanelEar, Nose, Throat
GMP ExemptYes

Identification

An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.

Classification Rationale

Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 874.9. If the device is not labeled or otherwise represented as sterile, it is exempt from the current good manufacturing practice requirements of the quality management system regulation in part 820 of this chapter, except for requirements concerning records and complaint files under § 820.35 of this chapter.

Recent Cleared Devices (4 of 4)

RecordDevice NameApplicantDecision DateDecision
K840311CAT. 7-EAR, NOSE & THROAT DEVICESImm Enterprises , Ltd.May 9, 1984SESE
K822754EAR/ULCER SYRINGEAmerican Hospital Supply Corp.Oct 4, 1982SESE
K810284AUTOMATIC TEFLON INJECTION SYRINGER. Wolf Medical Instruments Corp.Mar 11, 1981SESE
K780599SYRINGE, EAR & ULCERAbco Dealers, Inc.Apr 19, 1978SESE

Top Applicants

Innolitics

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