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

ENDOSCOPE SHEATH

K Number: K940028 · Decision Mar 24, 1995
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
12
Review Days
445

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
ENDOSCOPE SHEATH
K Number
K940028
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Xomed-Treace, Inc.
Date Received
January 3, 1994
Decision Date
March 24, 1995
Product Code
EOB
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
EOB Nasopharyngoscope (Flexible Or Rigid)

Similar 510(k) Clearances

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

View all

Other Clearances by Xomed-Treace, Inc.

K Number Device Name
K941407 TYMPANOSTOMY (VENTILATION) TUBE
K945659 BLACKSTAR(TM) STAR SYSTEM
K932771 BATTERY POWERED, DISPOSABLE ENDOSCOPE LIGHT SOURCE
K933672 XOMED-TREACE SCOPESHEATH
K934426 NERVE INTEGRITY MONITOR-2 (NIM-2 XL)
K933105 XOMED-TREACE RIGID ROD LENS ENDOSCOPE
K925640 XOMED-TREACE EMG ENDOTRACHEAL TUBEEN
K922880 XOMED TREACE JET VENTILATION TUBE
K923830 XOMED-TREACE ALPHASCOPE
K912753 XOMED-TREACE POSITROL FOOTPEDAL SUCTION CONTROL
Search all 12 clearances from Xomed-Treace, Inc. →