FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT

K Number: K925173 · Decision Jan 15, 1993
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
45
Applicant Total
9
Review Days
93

Basic Information

Device Name
BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT
K Number
K925173
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4780
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
WESTMED INTL.
Date Received
October 14, 1992
Decision Date
January 15, 1993
Product Code
LYA
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LYA Splint, Intranasal Septal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LYA), ordered by most recent decision date.

View all

Other Clearances by WESTMED INTL.

K Number Device Name
K955047 WESTMED CIRCULARIE PEP DEVICES
K954271 WESTMED CONDESATE COLLECTION TRAP
K952616 MICROTIME
K953687 WESTMED PEDIATRIC BACTERIAL/VIRAL FILTER
K953506 WESTMED RESPIRATORY LUER ADAPTOR
K951484 WESTMED BACTERIAL/VIRAL FILTER
K945472 WESTMED PEDIATRIC AND ADULT AEROSOL MASK
K924944 INSTANT IN-DWELL NASAL SUCT TAMP/ALLEVIA NASAL TRA