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

FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE

K Number: K895245 · Decision Nov 17, 1989
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
15
Review Days
88

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Basic Information

Device Name
FLEXIBLE FIBER-OPTIC NASOPHARYNGOSCOPE
K Number
K895245
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4760
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Applicant
Optimed Technologies, Inc.
Date Received
August 21, 1989
Decision Date
November 17, 1989
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.

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Other Clearances by Optimed Technologies, Inc.

K Number Device Name
K972520 OPTIVIEW
K955275 BOOSTER TROPHY 5 MOTORIZED SCOOTER
K955276 BOOSTER LITE 4 MOTORIZED SCOOTER
K955274 BOOSTER LITE 3 MOTORIZED SCOOTER
K943598 FLEXIBLE FIBER OPTIC LAPAROSCOPES
K926597 LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
K921942 HYSTEROSCOPE (AND ACCESSORIES)
K922711 FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE
K921985 ARTHROSCOPE & ACCESSORIES
K922826 FLEXIBLE FIBER OPTIC ENDOSCOPE
Search all 15 clearances from Optimed Technologies, Inc. →