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

BITE BLOCK/MOUTHPIECE FOR ENDOSCOPY

K Number: K915816 · Decision Mar 27, 1992
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
238
Applicant Total
8
Review Days
88

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Basic Information

Device Name
BITE BLOCK/MOUTHPIECE FOR ENDOSCOPY
K Number
K915816
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4680
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Gi Supply
Date Received
December 30, 1991
Decision Date
March 27, 1992
Product Code
EOQ
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
EOQ Bronchoscope (Flexible Or Rigid)

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K Number Device Name
K191923 EverLift Submucosal Lifting Agent
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K012411 HP-ONE
K970187 RUNYON LARGE VOLUME PARACENTESIS KIT
K970186 GI SUPPLY PARACENTESIS PUMP
K944903 HP-FAST
K931044 OXY-BLOC