FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VIDEO SCOPE SYSTEM (OTOSCOPE)

K Number: K944031 · Decision Sep 23, 1994
Classifications
1
FEI Numbers
228
Registration Numbers
228
Same Product Code
55
Applicant Total
92
Review Days
37

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Basic Information

Device Name
VIDEO SCOPE SYSTEM (OTOSCOPE)
K Number
K944031
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
874.4770
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jedmed Instrument Co.
Date Received
August 17, 1994
Decision Date
September 23, 1994
Product Code
ERA
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
ERA Otoscope

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Other Clearances by Jedmed Instrument Co.

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K954184 JED-LIGHT FIBEROPTIC LIGHT SOURCE
K944032 VIDEO SCOPE SYSTEM (LARYNGOSCOPE)
K950925 JEDMED LARYNGEAL SCOPE
K953457 JEDMED SPECTRUM ENT CABINET
K950785 HORTMANN AIRMATIC AIR CALORIC STIMULATOR
K950078 MICROFLOW IRRIGATION SYSTEM
K944671 VIDEO SCOPE SYSTEM (NASOPHARYNGOSCOPE {FLEXIBLE OR RIGID})
K941356 MICROFLOW IRRIGATION SYSTEM
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