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

HOOD PEDIATRIC TRACHEOSTOMY TUBE

K Number: K893866 · Decision Aug 7, 1989
Classifications
1
FEI Numbers
74
Registration Numbers
74
Same Product Code
127
Applicant Total
19
Review Days
73

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
HOOD PEDIATRIC TRACHEOSTOMY TUBE
K Number
K893866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5800
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Hood Laboratories
Date Received
May 26, 1989
Decision Date
August 7, 1989
Product Code
BTO
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
BTO Tube, Tracheostomy (W/Wo Connector)

Similar 510(k) Clearances

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

View all

Other Clearances by Hood Laboratories

K Number Device Name
K921452 ACOUSTIC RHINOMETER
K920994 HOOD NASAL SEPTAL BUTTON
K905703 KRUPIN EYE VALVE WITH DISK
K904821 ELIACHAR MODIFIED ESOPHAGEAL STENT
K897049 GIBSON ENDOLYMPHATIC SHUNT
K897059 HOOD SPEAKING VALVE
K884810 SILICONE LARYNGEAL STENT
K890599 HOOD NASAL SPLINT
K885125 KRUPIN EYE VALVE W/SCLERAL BUCKLE
K882430 HOOD TRACHEAL STOMA BUTTON
Search all 19 clearances from Hood Laboratories →