FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SHILEY FLEXTRA TRACHEOSTOMY TUBE

K Number: K030787 · Decision Nov 14, 2003
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
108
Applicant Total
42
Review Days
247

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SHILEY FLEXTRA TRACHEOSTOMY TUBE
K Number
K030787
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nellcor Puritan Bennett, Inc.
Date Received
March 12, 2003
Decision Date
November 14, 2003
Product Code
JOH
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
JOH Tube Tracheostomy And Tube Cuff

Similar 510(k) Clearances

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

View all

Other Clearances by Nellcor Puritan Bennett, Inc.

K Number Device Name
K070408 DURAMAX REUSABLE OXIMETRY SENSOR
K060576 NELLCOR OXIMAX N-600X PULSE OXIMETER
K051271 OXIMAX NEOMAX ADHESIVE FOREHEAD REFLECTANCE OXIMETRY SENSOR
K052186 NELLCOR OXIMAX PULSE OXIMETRY SENSONS (MAX-A, MAX-AL, MAX-N, MAX-I, MAX-P
K051352 OXIMAX NPB-40 HANDHELD PULSE OXIMETER
K050072 GOODKNIGHT 425ST
K033973 OXISENSOR II RECYCLED SENSOR AND OXIMAX RECYCLED SENSOR
K030930 OXIMAX SOFTCARE SENSORS, MODELS SC-A, SC-PR, SC-NEO, SC-N
K023494 NELLCOR INDGO MANUAL RESUSCITATOR
K022819 NELLCOR N-200 PULSE OXIMETER, MODEL N-200
Search all 42 clearances from Nellcor Puritan Bennett, Inc. →